$28.34 - Pharmaceris H Stimupurin, a specialist shampoo that stimulates hair growth, 250 ml — Made in Poland — Free Delivery

$28.34 - Pharmaceris H Stimupurin, a specialist shampoo that stimulates hair growth, 250 ml — Made in Poland — Free Delivery
Dr. Irena Eris #For_hair #Hair_shampoos #COSMETICS

Product description

The ingredients of the shampoo work at the cellular level by activating the genes responsible for the process of building new hair. At the same time, they stimulate the vital activity of the existing hair follicles, accelerating the natural growth of hair and extending its life cycle. Caffeine prevents genetically determined baldness by neutralizing the negative influence of hormones responsible for hair degradation and premature hair loss. Conditioning ingredients: niacinamide (vitamin PP), D-panthenol and biotin have a soothing effect, restoring the physiological balance of the scalp. The shampoo gently and effectively cleanses the hair and scalp. It smoothes the hair structure, strengthens and restores its natural density. It has a neutral pH for the skin. It helps to fight hair loss caused by genetics and hormones (androgenetic alopecia) and those caused by environmental factors. Effectively prevents hair loss resulting from long-term medication, stress, fatigue, weakening the body (diet) and after pregnancy. Safe for sensitive scalp.

Application

A shampoo designed especially for women and men with the problem of severe periodic and premature hair loss.

Usage method

Apply the appropriate amount of shampoo to hair, massage until lather, then rinse.

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$18.89 - Furoxin, 60 tablets — Made in Poland — Free Delivery

$18.89 - Furoxin, 60 tablets — Made in Poland — Free Delivery
LEK-AM #Urogenital_tract #Urinary_tract_infections #HEALTH_CARE

Product description

Furoxin is a modern preparation containing two natural ingredients: cranberry and nettle. Nettle extract supports the proper elimination of metabolic products and has a beneficial effect on maintaining the proper condition of the urinary tract.

Application

Supplementing the diet with ingredients contained in the product.

Recommended intake

Adults 1-2 coated tablets daily with meals.

Ingredients

Cranberry fruit extract (Vaccinum macrocarpon) containing 10% PACs, nettle leaf extract (Urtica dioica), microcrystalline cellulose (bulking agent), hydroxypropyl methylcellulose (glazing agent), polydextrose (bulking agent), talc (anti-caking agent), magnesium stearate anti-caking agent), silicon dioxide (anti-caking agent), titanium dioxide (dye), maltodextrin, medium chain triglycerides, red iron oxide (dye), carmines (dye).

1 coated tablet contains: 300 mg of cranberry fruit extract, including 30 mg PACs, 100 mg of nettle leaf extract.

Warnings

People with kidney problems, taking diuretics, pregnant and breastfeeding women should consult a doctor before using the preparation.

Important tips

Do not exceed the recommended daily dose.

A balanced diet and a proper lifestyle are important for the functioning of the human body.

A dietary supplement cannot be used as a substitute (replacement) for a varied diet.

The dietary supplement should be stored out of reach of small children.

The preparation should be stored at room temperature (15-25 degrees Celsius) in a dry place.

Do not use the preparation in case of hypersensitivity to any of the ingredients of the product.

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$18.89 - VALINGER 25MG, 4 TABS — MADE IN FINLAND — FREE SHIPPING

$18.89 - VALINGER 25MG, 4 TABS — MADE IN FINLAND — FREE SHIPPING
ORION PHARMA #Health #Potency #FOR_HIM

Product description

Valinger is a medicine that contains the active substance sildenafil, which works by helping to relax the blood vessels in the penis (the penis), thereby allowing blood to flow into the penis when you are sexually excited, thereby helping you to get an erection. The indication for the use of the preparation is the inability to obtain or maintain a penile erection, which prevents intercourse.

Indications

To treat erectile dysfunction known as impotence when you have problems getting or keeping a hard penis and making sexual activity impossible.

Composition

1 tablet contains:

• the active substance sildenafil 25 mg in the form of sildenafil citrate.
• excipients: tablet core: calcium hydrogen phosphate dihydrate, microcrystalline cellulose, magnesium stearate, colloidal anhydrous silica, sodium croscarmellose; shell: hypromellose (2910; 6 mPa ∙ s), titanium dioxide (E 171), macrogol 6000, talc, indigo carmine aluminum lake (E 132).

Action

Increasing blood flow to the penis by helping the blood vessels to relax.

Dosage

Use the medicine exactly as described in the package leaflet or as directed by your doctor or pharmacist. Please read the diagnostic tool in this leaflet before using the preparation.

• Adult men: 1 tablet (25 mg) daily, unless your doctor tells you otherwise.
• The tablet should be taken about 1 hour before planned sexual activity, swallowed whole with water.

This medicine will only help you to get an erection if you are sexually stimulated. The preparation usually works for half to one hour after taking it. Do not take more than 1 tablet a day. Do not use with other preparations containing sildenafil. If you have the impression that the effect of Valinger is too strong or too weak, talk to your doctor or pharmacist. If, after using the preparation, you do not get an erection or its duration is not sufficient for sexual activity, consult your doctor. Taking a dose higher than the recommended dose (over 100 mg) does not increase the effectiveness of the preparation. Contact your doctor if you take more tablets than recommended.

Contraindications

• Allergy to sildenafil or any of the other ingredients of the product.
• Taking nitrates.
• Use of preparations that release nitric oxide, including amyl nitrate.
• Taking riociguat.
• Serious heart or liver problems.
• Recent stroke, heart attack or low blood pressure.
• Certain rare inherited eye diseases, including retinitis pigmentosa.
• History of loss of vision due to non-arteritic anterior ischemic optic neuropathy (NAION).

Storage

• Keep the preparation out of the sight and reach of children.
• Medicines should not be disposed of via wastewater or household waste.
• Ask your pharmacist how to throw away medicines no longer needed. Such behavior will help to protect the environment.

Side effects

Valinger, like any other medicine, can cause side effects, but not everyone may experience them.

Stop taking the preparation immediately and contact your doctor if you experience the following serious side effects:

• an allergic reaction including sudden wheezing, difficulty in breathing or dizziness, swelling of the eyelids, face, mouth or throat
• chest pain (nitrates should not be used to relieve chest pain)
• excessively prolonged and sometimes painful erections (if an erection lasts more than 4 hours, contact your doctor immediately),
• sudden deterioration or loss of vision,
• severe skin reactions including severe peeling and swelling of the skin, blistering of the mouth, genitals and around the eyes, fever
• seizures or fits or fainting.

Very common (may affect more than 1 in 10 people):

• Headache.

Common (may affect up to 1 in 10 people):

• nausea,
• flushing, flushing
• indigestion,
• blurred vision,
• stuffy nose
• dizziness.

Uncommon (may affect up to 1 in 100 people):

• vomiting,
• skin rash
• eye irritation, redness of the eyes, eye pain, seeing flashes of light, vivid vision, sensitivity to light, watery eyes,
• palpitations, rapid heartbeat, high blood pressure, low blood pressure,
• muscle pain, sleepiness, reduced sense of touch
• dizziness, ringing in the ears
• dry mouth
• blocked or obstructed sinuses, rhinitis
• upper stomach pain, gastro-oesophageal reflux disease (symptoms include heartburn)
• blood in urine
• pain in arms or legs
• epistaxis,
• feeling hot and tired.

Rare (may affect up to 1 in 1,000 people):

• fainting, stroke, heart attack, irregular heartbeat, temporary reduction in blood flow to part of the brain
• throat tightness, numbness in the mouth,
• bleeding in the back of the eye, eye irritation, retinal disease caused by atherosclerosis, iris disorder, double vision, decreased visual acuity, abnormal sensation inside the eye, swelling of the eyes or eyelids, increased intraocular pressure (glaucoma), myopia, eyestrain, small particles or points in the field of view, seeing a halo around light sources (halo effect), pupil dilation, discoloration of the eye's protein
• penile bleeding, blood in semen
• dry nose, swelling inside the nose
• feeling irritable, and sudden loss or loss of hearing.

Other possible side effects:

• unstable angina (heart disease), sudden cardiac death.

Interactions

Tell your doctor and / or pharmacist about all the preparations you are taking or are taking.

• Valinger may interact with some medications, especially those taken to treat chest pain.
• Do not take Valinger with other medicines, unless your doctor agrees.
• In the event of an event requiring immediate medical attention, inform your doctor that you have taken Valinger and when you have taken it.
• If you are taking protease inhibitors used to treat HIV infection, it is recommended that you start treatment with the lowest dose (25 mg) of Valinger.
• Taking Valinger with alpha blockers at the same time may cause dizziness or light headedness, most likely to occur within 4 hours of taking Valinger.
• Valinger can be taken with or without food (eating a heavy meal may extend the time it takes to start working).
• Drinking alcohol may temporarily impair your ability to get an erection (do not drink large amounts of alcohol before taking this medicine).
• Valinger may cause dizziness and visual disturbances which should be taken into account when driving or operating machinery.
• It is essentially "sodium-free" (contains less than 1mmol / 23mg sodium per tablet).

Warnings and Precautions

A doctor and / or pharmacist should be consulted before using the preparation in the event of:

• have sickle cell anemia, leukemia, multiple myeloma,
• anatomical deformity of the penis or Peyronie's disease,
• heart problems
• stomach ulcer or bleeding disorders.

In the event of a sudden decrease in vision or sudden loss of vision, stop taking this medicine and consult your doctor immediately.

Valinger should not be used concomitantly with other oral or local treatments for erectile dysfunction.

The use of the preparation is not recommended in people without erectile dysfunction.

The preparationis not intended for use by women.

Valinger should not be used concomitantly with preparations for the treatment of pulmonary arterial hypertension (PAH) containing sildenafil or other PDE5 inhibitors.

Patients with kidney or liver disorders should not use a dose higher than 25 mg and consult a doctor before taking the preparation.

The preparationshould not be used in people under 18 years of age.

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$27.92 - ENGYSTOL INJECTION FOR AMPOULES 1.1ML 5pcs — MADE IN GERMANY — FREE SHIPPING

$27.92 - ENGYSTOL INJECTION FOR AMPOULES 1.1ML 5pcs — MADE IN GERMANY — FREE SHIPPING
Heel #Homeopathy #HEALTH_CARE

ENGYSTOL INJECTION FOR AMPOULES

The preparation (in the form of injections) has an immunocorrective (indirect antiviral), anti-inflammatory, detoxifying, regenerating sh-group of enzymes in intoxication, which is based on the activation of the body's defenses and normalization of its functions.

Ingredients:

active substances: 1.1 ml of solution contain: Sulfur D4 - 3.3 μl, Sulfur D10 - 3.3 μl, Vincetoxicum hirundinaria D6 - 6.6 μl, Vincetoxicum hirundinaria D10 - 6.6 μl, Vincetoxicum hirundinaria D30 - 6.6 μl;

Excipients:

sodium chloride, water for injections.

Indications

Acute and chronic infectious diseases of viral origin (hepatitis, cytomegalovirus infection, herpes, bronchitis, pneumonia, whooping cough, influenza, SARS); neurodermatitis, eczema, endocarditis, myocarditis, kidney disease, rheumatic diseases.

Application

Single dose: adults and children over 6 years - 1 ampoule of 1.1 ml. Apply 1-3 times a week in the form of intravenous, intravenous, intravenous (acupuncture points), intravenous (jet) injections. In acute cases - 1 ampoule daily for 3-5 days.
The course of treatment is 2-5 weeks.

Contraindications

Hypersensitivity to any of the components of the preparation.

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$38.84 - Intelaria 30 capsules — Made in Spain — Free Deliveryes

$38.84 - Intelaria 30 capsules — Made in Spain — Free Deliveryes
HC Clover #The_nervous_system #Memory_and_concentration #HEALTH_CARE

Product description

The Intelaria complex is used as a dietary supplement, as a source of structural phospholipids phosphatidylserine and phosphatidylcholine, natural polyphenol resveratrol and polyunsaturated omega-3 fatty acids (docosahexaenoic and eicosapentaenoic) with the aim of improving cognitive (cognitive) functions, memory, decreased attention in persons with age chronic impairment of cerebral circulation, neurodegenerative changes; normalization of the psycho-emotional state and reduction of stress caused by intense mental work or physical training.

Active ingredients

Intelaria is a balanced complex of structural phospholipids, soluble in omega-3 fatty acids, to maintain and improve memory, attention, thinking and reduce stress in people with age-related decline in brain function, cerebrovascular accident and intense strenuous work.

Phosphatidylserine (PS) is a structural phospholipid component of the inner layer of the cell membrane of the brain, which ensures the normal functioning of nerve cells; improves electrical conduction between neurons, release of neurotransmitters, protection and restoration of brain cells.

Phosphatidylserine helps to increase the production of the neurotransmitter acetylcholine, which is necessary for attention, learning and memory; stimulating the release of dopamine - a mood regulator; increased glucose metabolism in brain cells - a source of energy for brain activity; a decrease in the level of cortisol - a stress hormone, reduces the degree of mental and physical stress; increased activity of nerve growth factor (NGF), which controls the formation of brain cells, maintains their activity and viability; reduction of excessive activity of the ß-rhythm, promotes relaxation and simultaneous concentration of attention.

When taking PS, it quickly overcomes the blood-brain barrier, accumulates in brain cells and has a beneficial effect on brain activity.

Phosphatidylcholine (PC), a structural phospholipid component of cell membranes, in particular, the outer layer of the brain cell membrane, is a source of choline, which is necessary for the synthesis of the important neurotransmitter acetylcholine, which ensures the transmission of nerve impulses between neurons. PC improves cognitive functions of the brain, liver function, participates in metabolic processes, reduces the absorption of cholesterol from foods and the formation of fatty deposits.

Resveratrol is a naturally occurring polyphenol found in grapes, wine, and Japanese mountaineers. Due to its powerful antioxidant, anti-inflammatory properties, it has a neuroprotective effect, helps to increase the availability of nitric oxide in the vascular wall, improves cerebral blood flow, activates metabolic processes and prevents the formation of amyloid in brain cells, protects against aging and degenerative processes.

Docosahexaenoic acid (DHA) and eicosapentaenoic acid (EPA) are the most abundant omega-3 polyunsaturated fatty acids in the brain and are important structural and functional components of the nervous system. DHA and EPA provide neurogenesis, neurotransmission, neuroprotection and protection against oxidative stress of brain tissue. DHA synthesizes a docosanoid - neuroprotectin D1, which has a neuroprotective, anti-inflammatory and anti-apoptotic effect, helps to reduce the degree of neuronal damage during trauma, ischemia and toxic damage to the central nervous system.

Advantages

• stimulates the brain;
• helps to improve thinking processes, concentration of attention, memory;
• increases the resistance of brain cells to ischemic damage;
• prevents aging of brain cells.

Indications for use

The Intelaria / Intelaria complex is used as a dietary supplement, as a source of structural phospholipids phosphatidylserine and phosphatidylcholine, natural polyphenol resveratrol and polyunsaturated omega-3 fatty acids (docosahexaenoic and eicosapentaenoic) with the aim of improving cognitive (cognitive) functions in the brain, memory, memory functions, chronic disturbance of cerebral circulation, neurodegenerative changes; normalization of the psycho-emotional state and reduction of stress caused by intense mental work or physical training.

Contraindications

Do not exceed the recommended daily dose. Should not be used as a substitute for a varied diet. Use with caution with preparations that increase the level of acetylcholine, such as acetylcholinesterase inhibitors. Very rarely, dyspeptic disorders, headache, allergic reactions can be observed. Before starting use, it is recommended to consult a doctor. Do not use for children.

Mode of application

Adults - 1 capsule 2 times a day, regardless of food intake.

Composition

active ingredients: fish oil (eicosapentaenoic acid - 90 mg (mg) docosahexaenoic acid - 60 mg (mg)) - 500 mg (mg) soy lecithin (phosphatidylcholine - 64 mg (mg)) - 200 mg (mg), phosphatidylserine - 110 mg (mg) Japanese knotweed extract 50% (resveratrol - 10 mg (mg)) - 20 mg (mg);

excipients: capsule shell: gelatin; emulsifier: glycerin antifoam: yellow bjolinium wax; dyes: brown iron oxide, black iron oxide, red iron oxide.

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$45.14 - 1 Day Acuvue Moist for Astigmatism (30 Lenses) DIA 14.50, BC 8.50 — Made in USA — Free Delivery

$45.14 - 1 Day Acuvue Moist for Astigmatism (30 Lenses) DIA 14.50, BC 8.50 — Made in USA — Free Delivery
Johnson & Johnson #Eyes #Contact_lenses #One_day #HEALTH_CARE

1 Day Acuvue Moist for Astigmatism contact lenses

Johnson & Johnson introduced daily disposable contact lenses for people with astigmatism with the 1 Day Acuvue Moist contact lens range. These lenses have an innovative structure, and the modern LACREON Technology™ technology was used in their production, which offers the widest range of parameters on the market of one-day toric contact lenses. According to the manufacturer, these lenses work 95% of the time on the first fit.

LACREON Technology™

1 Day Acuvue Moist for Astigmatism uses the innovative LACREON™ technology, which retains a highly moisturizing substance imitating natural tears inside the lens. Thanks to this, the eyes are properly moisturized and fresh for the entire duration of wearing the lenses.

ASD technology

The unique four-zone stabilization system uses the natural pressure in the eyelids so that the lens does not move even when blinking. This allows the user to see clearly all day long. This solution also facilitates the insertion of the lens, which immediately adapts to the eye.

1 Day Acuvue Moist for Astigmatism provides high wearing comfort, eye protection against UV-A and UV-B radiation and is an excellent solution for toric contact lens wearers. The manufacturer informs that these lenses block approx. 98% of UV-B radiation and 85% of UV-A radiation.

The "inside out mark" on the lenses will help you check that the lenses are inserted the right way around. The easiest way to see the marking is by looking at the lens from the side

Features - 1 Day Acuvue Moist for Astigmatism (30 Lenses)

Producer: Johnson and Johnson

Dia: 14.50

BC: 8.50

Package size: 30 lenses

Replacement schedule: 1 Day

Product name: 1 Day Acuvue Moist for Astigmatism

Importance: 12 months and more

Oxygen permeability: 23.7 Dk/t

Water content: 58%

Lens material: Etafilcon A

cylinder power: from -0.75 to -2.25

Power Range: from -9.00 to +4.00

For night / continuous wear: NO

UV filter: Yes

Medical component: Yes

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$18.89 - Destresan night with melatonin 24 capsules — Made in Poland — Free Delivery

$18.89 - Destresan night with melatonin 24 capsules — Made in Poland — Free Delivery
OLEOFARM #The_nervous_system #Insomnia #HEALTH_CARE

Product description

Destresan night with melatonin dietary supplement contains a composition of plant extracts: lemon balm leaves and common hops enriched with magnesium, vitamin B6 and melatonin. The recommended daily dose contains 1 mg of melatonin, the amount consumed shortly before going to bed helps to reduce the time needed to fall asleep. Lemon balm has a calming effect, and hops soothe and support restful sleep. Magnesium and vitamin B6 help in the proper functioning of the nervous system.

Application

Supplementing the diet with active ingredients of the preparation.

Recommended intake

Adults: 1 capsule a day, half an hour before bedtime.

Ingredients

Lemon balm leaves extract (Melissa officinalis), hops extract (Humulus lupulus), magnesium oxide, gelatin (shell component), anti-caking agent: magnesium salts of fatty acids, anti-caking agent: silicon dioxide, pyridoxine hydrochloride, melatonin, dye: titanium dioxide, color: indigo carmine.

1 capsule contains: lemon balm leaf extract 200 mg, hops extract 150 mg, magnesium 56.25 mg (15%) *, vitamin B6 1.4 mg (100%) *, melatonin 1 mg

* RWS - Reference Value of Consumption.

Warnings

Pregnant and breastfeeding women should consult a doctor before consuming the preparation. Preparations containing melatonin may impair concentration and reaction speed, and affect the ability to drive vehicles and operate moving mechanisms. Do not drink alcohol while using the preparation.

Important tips

Do not exceed the recommended daily dose.

A balanced diet and a proper lifestyle are important for the functioning of the human body.

A dietary supplement cannot be used as a substitute (replacement) for a varied diet.

Store in a dry and dark place at room temperature, out of reach of small children.

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$17.84 - Lucetam 1200mg 20 tablets — Made in Hungary — Free Delivery

$17.84 - Lucetam 1200mg 20 tablets — Made in Hungary — Free Delivery
EGIS #The_nervous_system #Nervous_system_support #HEALTH_CARE

Product description

Lucetam (Piracetamum, Piracetam) - neuroprotective preparations.

Piracetam - cyclic derivative of GABA. Direct impact on the brain. Lucetam improves cognitive (cognitive) processes, such as learning ability, memory, attention, ability to memorize, as well as improves mental performance, without the development of sedative and psychostimulant effect.

Has impact on the central nervous system in various ways: change the speed of propagation of excitation in the brain, improves neuronal plasticity and metabolic processes in the nerve cells. It improves the interaction between the hemispheres of the brain and synaptic conductance in neocortical structures, it improves mental performance, improves cerebral blood flow.

Lucetam improves microcirculation in the brain, affecting the rheological properties of blood and causes vasodilatory action. Lucetam inhibits platelet aggregation and restores the elasticity of erythrocyte membranes, as well as the ability of the latter to the passage through the microcirculation. It reduces adhesion of red blood cells. At a dose of 9.6 g reduces levels of fibrinogen and von Willebrand factor by 30-40% and prolongs bleeding time.

Lucetam has a protective and restorative action in violation of brain function due to hypoxia, intoxication or injury. It reduces the severity and duration of vestibular nystagmus.

Testimony:

• Symptomatic treatment of psycho-organic syndrome, particularly in elderly patients suffering from memory loss, concentration and total activity, dizziness, mood changes, conduct disorder, gait disorder, as well as in patients with Alzheimer's disease and senile dementia of the Alzheimer type.
• Treatment of the consequences of ischemic stroke as speech disorders, disorders of the emotional sphere, motor and mental activity.
• Chronic alcoholism - for the treatment of psycho-organic and withdrawal syndromes.
• During the recovery period after injuries and cerebral intoxication.
• Treatment of vertigo and associated disorders of balance, with the exception of dizziness psychic origin.
• In the complex treatment of lower learning in children, especially in the case of difficulty of acquisition of specific skills of reading, writing, numeracy, which can not be explained by mental retardation, inadequate training or feature family environment.
• For the treatment of cortical myoclonus as mono- or combination therapy.

Contraindications:

• Hemorrhagic stroke.
• End-stage renal failure (creatinine clearance at least 20 ml / min).
• Children under the age of 1 year.
• Pregnancy.
• Lactation.
• Hypersensitivity to piracetam or pyrrolidone derivatives, and other ingredients.

Pregnancy and breast-feeding:

Animal studies have not revealed the damaging effect on the embryo and the development of the offspring, including in the postnatal period, and did not change during pregnancy and childbirth. Studies have not been conducted in pregnant women. Piracetam crosses the placental barrier and into breast milk. The concentration of the preparation in infants up to 70-90% of its concentration in the blood of the mother. Except in special circumstances Lutsetam should not be administered during pregnancy. It should refrain from breast-feeding in the appointment of a woman Lutsetam.

Special instructions:

In connection with the effect of piracetam on platelet aggregation caution should be prescribed to patients with impaired hemostasis during major surgery or in patients with symptoms of severe bleeding.

In the treatment of cortical myoclonus abrupt interruption of treatment should be avoided, which might cause the resumption of seizures.

It penetrates through the filtration membranes for hemodialysis machines.

When long-term therapy of elderly patients are advised to regularly monitor indicators of kidney function, if necessary, shall adjust the dose depending on the results of research spacecraft.

Taking into account possible side effects, the patient should be careful when driving and operating machinery.

Suggested Use:

Inside the preparation is administered in a daily dose of 30-160 mg / kg, the multiplicity of reception - 2-4 times / day.

Lutsetam tablets taken with meals or on an empty stomach, with some liquid (water, juice).

administered 1.2-2.4 g / day, and during the first week in the symptomatic treatment of chronic psycho-organic syndrome depending on the severity of symptoms - 4.8 g / day.

In the treatment of the effects of stroke appoint 4.8 g / day.

When alcohol withdrawal syndrome - 12 g / day. The maintenance dose - 2.4 g / day.

For the treatment of vertigo and associated disorders of balance administered 2.4-4.8 g / day.

When cortical myoclonus treatment starts with a dose of 7.2 g / day, once every 3-4 days, increase the dose of 4.8 g / day to a maximum dose of 24 g / day. Treatment continued throughout the period of the disease. Every 6 months should attempt to reduce the dose or stop the preparation, gradually reducing the dose of 1.2 g every 2 days in order to prevent an attack. In the absence of treatment effect or a slight therapeutic effect is stopped.

Babies for the correction of learning disabilities prescribed oral dose of 3.2 g / day. Treatment continues throughout the school year.

In patients with impaired function of the liver correction mode is not required.

In patients with impaired renal function requires correction dosing regimen according to creatinine clearance (CC). The degree of renal failure QC (ml / min) Dose Rate of> 80 Usual dose Light 50-79 2/3 usual dose is 2 - 3 admission average 30-49 1/3 usual dose in 2 hours Weight <30 1/6 usual dose, End-stage single - contraindicated

In elderly patients a dose of correcting the presence of renal insufficiency and long-term treatment is necessary to monitor renal function.

Packaging:

• Comes in original packaging. Item is brand new and unopened.

Storage:

• Keep away from direct sunlight.
• Keep locked and away from children.
• Store in dry place at room temperature.
• Do not exceed storage temperature higher than 25 C

Important notice- the outer box design may vary before prior notice!

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$17.84 - Torasemide-Teva 5mg 30 tablets — Made in Spain — Free Delivery

$17.84 - Torasemide-Teva 5mg 30 tablets — Made in Spain — Free Delivery
TEVA #Urogenital_tract #Urolithiasis #HEALTH_CARE

Pharmacological properties

Pharmacodynamics. Torasemide is a loop diuretic that inhibits renal reabsorption of sodium and chlorine ions in the ascending part of the henle loop. However, in low doses, the pharmacodynamic profile of torasemide in the degree and duration of diuresis brings it closer to the thiazide class. in high doses, torasemide provides diuresis with dose-dependent intensity and a high limit of effect. The maximum diuretic activity of torasemide is achieved 2-3 hours after oral administration. In healthy volunteers, doses of 5–100 mg caused a logarithmic increase in diuretic activity. The antihypertensive effect of torasemide is associated with a decrease in the ovarian pressure due to a decrease in patients with arterial hypertension of the increased activity of free ca2 + in the cells of the muscle layer of the arteries. as a result of this, contractility and the reaction of the vessels to the body's own pressor substances, for example, catecholamines, are probably reduced.

Pharmacokinetics. After oral administration, torasemide is rapidly and almost completely absorbed in the gastrointestinal tract. Cmax in blood plasma is achieved within 1–2 hours. Systemic bioavailability after oral administration is 80–90%. More than 99% of torasemide binds to blood plasma proteins, and the binding to proteins of metabolites M1, M3 and M5 is 86, respectively; 95 and 97%. The volume of distribution reaches 16 liters. During the metabolism of torasemide due to stepwise oxidation, hydroxylation or ring hydroxylation, three metabolites are formed - M1, M3 and M5. Hydroxyl metabolites are diuretic. The share of metabolites M1 and M3 accounts for about 10% of the pharmacodynamic action, and the metabolite M5 is inactive.

In healthy volunteers, the final T½ of torasemide and its metabolites is 3-4 hours. The total clearance of torasemide reaches 40 ml / min, and the renal clearance is about 10 ml / min. Approximately 80% of the dose is excreted by the renal tubules in the form of torasemide and its metabolites: torasemide - 24%, M1 - 12%, M3 - 3%, M5 - 41%. In case of impaired renal function, the T½ of torasemide does not change, but the T½ of the metabolites M3 and M5 increases. Hemodialysis and hemofiltration do not significantly remove torasemide and its metabolites. If in patients with impaired renal function there is an increase in the concentration of torasemide in the blood plasma, then this is most likely a consequence of a weakening of hepatic metabolism. In patients with heart failure or impaired liver function, the T½ of torasemide and the M5 metabolite increases slightly, but accumulation is unlikely.

Indications

Essential ag. swelling and / or effusion caused by congestive heart failure.

Application

Essential ag: the recommended dose of torasemide is 2.5 mg (½ torasemide-teva tablet 5 mg) once a day. if necessary, the dose can be increased to 5 mg / day. the use of doses of 5 mg / day does not cause an additional decrease in blood pressure. the maximum hypotensive effect is achieved after about 12 weeks of continuous treatment.

Edema: the usual recommended dose is 5 mg once a day. This is usually a maintenance dose. If necessary, the dose can be gradually increased to 20 mg once a day.

Elderly patients. Use with caution, since there is insufficient information about the need for dose adjustment for elderly patients.

Patients with impaired liver and kidney function. Information on dose adjustment in patients with impaired liver and kidney function is limited. In patients with impaired liver function, it should be used with caution, since an increase in the concentration of torasemide in the blood plasma is possible.

Reception method. Used internally. Torasemid-Teva tablets should be used in the morning, without chewing, with a small amount of liquid. Bioavailability of Torasemid-Teva does not depend on food intake. The duration of treatment depends on the course of the disease.

Children. Safety and efficacy in children have not been established, therefore, torasemide should not be prescribed to this age group of patients.

Contraindications

Hypersensitivity to torasemide, sulfonylurea or any component of the drug. impaired renal function, accompanied by anuria, impaired urination. disorders of urination (for example, benign prostatic hyperplasia). hepatic coma and precoma. arterial hypotension. arrhythmia (for example, sinoatrial blockade, av-block II – III degree). hypokalemia, hyponatremia, hypovolemia.

Side effects

From the side of metabolism: violations of water and electrolyte balance (especially with a noticeable restriction of salt in the diet), hypokalemia (especially in the case of insufficient potassium in the diet, as well as vomiting, diarrhea, frequent use of laxatives and liver dysfunction); an increase in the level of uric acid, glucose and lipids in the blood plasma; exacerbation of metabolic alkalosis, hyperuricemia, hypovolemia, hyponatremia.

With a sufficiently strong diuresis, especially at the initial stage of treatment and in elderly patients, symptoms and signs of a decrease in the amount of electrolytes and their volume may occur, for example, headache, dizziness, arterial hypotension, weakness, drowsiness, confusion, loss of appetite and convulsions. Dose adjustment is required.

From the side of the cardiovascular system: thromboembolic complications; cardiac and cerebral ischemia, which can lead, in particular, to cardiac arrhythmias, angina pectoris, acute myocardial infarction or fainting; extrasystole, palpitations, tachycardia.

From the digestive system: loss of appetite, stomach pain, nausea, vomiting, diarrhea, constipation, pancreatitis, flatulence.

From the side of the kidneys and urinary tract: urinary retention in patients with urinary tract obstruction, urgent urge to urinate, increased levels of creatinine and urea in the blood plasma.

From the hepatobiliary system: an increase in the level of certain liver enzymes, for example, gamma-glutamyl transpeptidase.

On the part of the blood and lymphatic system: a decrease in the number of erythrocytes, leukocytes and platelets.

On the part of the skin and subcutaneous tissues: allergic reactions, including rash, itching, photosensitivity, severe skin reactions.

From the nervous system: headache, dizziness, fatigue, weakness, paresthesia of the extremities, drowsiness, increased activity, nervousness.

From the respiratory system: nosebleeds.

Others: asthenia, dry mouth, thirst, blurred vision, tinnitus, deafness.

Special instructions

Treatment with torasemid-teva should be started after correction of hypokalemia, hyponatremia and hypovolemia.

Dysfunction of the kidneys and liver. So far, limited information has been collected on dose adjustment in patients with impaired renal and hepatic function. Care should be taken to treat patients with impaired liver function, since it is possible to increase the concentration of the drug in the blood plasma. Torasemide should be used with extreme caution in patients with liver disease, accompanied by cirrhosis and ascites, since sudden changes in water and electrolyte balance can lead to hepatic coma. Therapy with torasemide (as well as other diuretics) for patients of this group should be carried out in a hospital setting. To prevent hypokalemia and metabolic alkalosis, the drug should be prescribed with drugs - aldosterone antagonists or potassium-sparing drugs.

With long-term diuretic treatment, it is recommended to regularly assess the balance of electrolytes (in particular in patients with concomitant therapy with digitalis glycosides, GCS, mineralocorticoids or laxatives), glucose, uric acid, creatinine and blood lipids, as well as blood cells (erythrocytes, leukocytes and platelets) ...

Careful monitoring of patients with a tendency to hyperuricemia and gout is recommended. Blood glucose control is necessary for latent or severe diabetes. Due to the lack of sufficient experience in clinical use, it is not recommended to prescribe torasemide for:

• pathological changes in acid-base balance;
• concomitant use of lithium, aminoglycosides or cephalosporins;
• impaired renal function caused by nephrotoxic agents;
• pathological changes in the blood (for example, thrombocytopenia or anemia in patients without impaired renal function).

Torasemid-Teva tablets contain lactose. The drug should not be used in patients with rare hereditary galactose intolerance, lactase deficiency or glucose-galactose malabsorption syndrome.

Use during pregnancy and lactation. There is no data on the effect of torasemide on the embryo and fetus. Animal studies have shown no fetal or maternal toxicity after high doses. Torasemide penetrates the fetal membrane and causes electrolyte disturbances. There is also a risk of neonatal thrombocytopenia.

During pregnancy, the drug is used only when the expected benefit to the mother significantly outweighs the risk to the fetus. In this case, the lowest possible dose should be used. There are currently no data on the penetration of torasemide into breast milk. Torasemide is contraindicated for use during lactation.

The ability to influence the reaction rate when driving or working with other mechanisms. As in the case of other drugs that affect blood pressure, patients using torasemide should not drive vehicles and work with mechanisms that require concentration of attention, since dizziness and other associated symptoms may occur. This is especially true when starting treatment, increasing dosage and switching to other drugs.

Interactions

When combined with cardiac glycosides, a deficiency of potassium or magnesium can increase the sensitivity of the heart muscle to these drugs. with the simultaneous use of torasemide with mineral and glucocorticoids, laxatives, the excretion of potassium may increase.

With the simultaneous use of torasemide enhances the effect of antihypertensive drugs, in particular ACE inhibitors.

Sequential or combination therapy, as well as the beginning of a new concomitant therapy with an ACE inhibitor, can cause severe arterial hypotension. It can be reduced by lowering the initial dose of the ACE inhibitor or by reducing the dose / temporarily discontinuing the drug 2 or 3 days before starting the ACE inhibitor.

Torasemide can reduce the sensitivity of the arteries to vasoconstrictors, such as epinephrine, norepinephrine.

Torasemide is able to weaken the effect of antidiabetic drugs.

Torasemide, especially in high doses, can enhance the nephrotoxic and ototoxic effects of aminoglycoside antibiotics and ethacrynic acid, especially in patients with renal insufficiency; the toxicity of cisplatin drugs and the nephrotoxic effect of cephalosporins.

It is also possible to enhance the action of theophylline and muscle relaxants based on curare.

NSAIDs (eg indomethacin) can reduce the hypotensive and diuretic effect of torasemide, probably due to inhibition of prostaglandin synthesis.

Probenecid reduces the effectiveness of torasemide due to inhibition of tubular secretion.

An increase in plasma concentrations of lithium is possible, as well as an increase in the severity of its cardio- and neurotoxic effects.

Torasemide inhibits the excretion of salicylates by the kidneys, which increases the risk of their toxicity in patients using high doses of salicylates.

With the simultaneous use of torasemide and cholestyramine, the absorption of torasemide may decrease, thereby weakening the effect of the latter.

Overdose

Symptoms in case of an overdose, an increase in side reactions (strong diuresis, causing dehydration, hypovolemia, arterial hypotension, hyponatremia, hypochloremic alkalosis, hemoconcentration, drowsiness, confusion, cardiovascular failure, loss of consciousness) is possible. possible gastrointestinal disturbances.

Treatment. The specific antidote is unknown. Symptoms and signs of an overdose may necessitate a dose reduction or discontinuation of Torasemid-Teva with a parallel restoration of fluid and electrolyte balance and symptomatic treatment.

Storage conditions

At a temperature not exceeding 30°c.

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$19.94 - INNOFER BABY SUSPENSION 50ML - MADE IN POLAND - FREE SHIPPING

$19.94 - INNOFER BABY SUSPENSION 50ML - MADE IN POLAND - FREE SHIPPING
Smart Pharma #Child_health #Vitamins_and_minerals_for_children #Iron #CHILD

Product description

Innofer baby is indicated for the dietary management of iron deficiency and iron deficiency anemia.

The preparation contains elemental iron which:

- has the GRAS (Generally Recognized As Safe) safety status, awarded by the US Department of Health; signifying that the substance, on the basis of many studies, has been generally recognized as safe;

- according to studies conducted also on infants and children, it does not cause side effects such as constipation, diarrhea or abdominal pain. In addition, it does not oxidize in the mouth, so it does not stain the teeth and has no metallic aftertaste;

- is at zero oxidation state and oxidizes in the stomach under the influence of hydrochloric acid to easily digestible divalent ions. The conversion to the ionic form is spread over time and proceeds in a gentle manner, without causing excess ions that irritate the mucosa;

- has a very high bioavailability at the level of 69%, which, combined with the precision of dosing, guarantees that it will be absorbed and will not cause a dangerous excess of free ions

Application

For the dietary management of iron deficiency and iron deficiency anemia. Intended for newborns and infants, especially premature babies with low birth weight and children.

Recommended intake

The dosage and duration of use depend on the degree of iron deficiency and should be carried out according to the doctor's recommendations and under his supervision.

Before use, to obtain a homogeneous suspension, the product should be thoroughly mixed. To do this, shake the bottle vigorously for no less than 30 seconds until a dark color is obtained. It is recommended to shake the bottle vigorously before each dose is withdrawn, even if administration is within 3 minutes of obtaining a homogeneous suspension. The measured dose should be administered directly into the mouth immediately after preparation.

0.1ml = 1mg iron

1 ml = 10 mg iron

Ingredients

MCT vegetable oil (Medium Chain Triglycerides), elemental iron.

100ml of the preparation contains:

- energy value 3346kJ / 793kcal

- 96g fat, including 96g saturated fatty acids, monounsaturated fatty acids less than 0.1g, 0g polyunsaturated fatty acids, 0g carbohydrates, including 0g sugars, 0g protein, salt less than 0.01g, iron 1000mg (7143%) *

1 ml of the preparation contains:

- 34kJ / 8kcal energy value

- fat 1g, including saturated fatty acids 1g, monounsaturated fatty acids less than 0.1g, polyunsaturated fatty acids 0g, carbohydrates 0g, including sugars 0g, protein 0g, salt less than 0.01g, iron 10mg (71.4% ) *

* RWS - Reference Value of Consumption.

Contraindications

Do not use in case of hypersensitivity to any component of the product. It is not intended for parenteral use.

Important tips

Do not exceed recommended servings for consumption during the day.

The product cannot be used as a substitute for a varied diet and a healthy lifestyle.

A balanced diet. A proper lifestyle is important for the functioning of the human body.

Store in a dry place at a temperature not exceeding 25 ° C in the original package in order to protect from light.

Do not expose the product to heat, sunlight or moisture.

Keep out of reach of children.

After first opening, the product should be used within 90 days.

It is intended for use under medical supervision.

It does not contain cow's milk proteins, lactose, gluten and can be administered to people who do not tolerate these ingredients

It does not contain preservatives, dyes and sweeteners

Does not stain teeth.

It may pose a health risk if consumed by people for whom there are no medical indications for its administration.

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$52.49 - 3 x BIOTEBAL EYELASHES XXL SERUM 3ML - MADE IN POLAND - FREE SHIPPING

$52.49 - 3 x BIOTEBAL EYELASHES XXL SERUM 3ML - MADE IN POLAND - FREE SHIPPING
POLPHARMA #For_eyelashes_and_eyebrows #COSMETICS

BIOTEBAL EYELASHES XXL SERUM 3ML

Biotebal eyelashes XXL, serum stimulating eyelash growth.

Composition according to INCI

Aqua, Glycerin, Disodium Phosphate, Panthenol, Biosaccharide Gum-1, Biotinoyl Tripeptide-1, Biotin, Bimatoprost, Euphrasia Officinalis Extract, Hydrolyzed Cucurbita Pepo Seedcake, Propylene Glycol, Xanthan Gumpar, Imidazolidinyl UTA, Citric Acididium EDabrea, Dishodyl Acididium EDabrea, Metricyl Acididium EDabrea, The dead man.

Capacity

3 ml

Usage method

Use once a day at night.

Properties

Biotebal Eyelashes XXL is a specialized serum that after 3 weeks of use provides the effect of long, beautiful and healthy eyelashes. Thanks to the special Inno-BiBiotin ™ formula, it effectively and safely lengthens, thickens and strengthens eyelashes and eyebrows. It contains bimatoprost - known and considered in the world today as one of the most effective ingredients stimulating the growth of eyelashes and inhibiting the process of their loss, and ingredients of plant origin with soothing properties.

Comments

Do not use in case of eye diseases or hypersensitivity to any component of the product.

Biotebal  XXL is a specialized serum that provides the effect of long, beautiful and healthy eyelashes after just 3 weeks of use. Thanks to the special Inno-BiBiotinTM formula, it effectively and safely lengthens, thickens and strengthens eyelashes and eyebrows.

Contains tested, active ingredients:

Bimatoprost - known and considered in the world today as one of the most effective ingredients stimulating the growth of eyelashes and inhibiting the process of their loss. If used regularly, it makes lashes longer, thicker and stronger. They are more flexible, shiny and take on a darker color.

Biotin - vitamin H - has a beneficial effect on the condition of the hair and its growth rate. It is an effective means of stimulating the growth of eyelashes and eyebrows.

Panthenol - provitamin B5 - plays an important role in hair care, giving it shine and softness. It smoothes and thickens the hair fiber, protects against damage. It has a regenerating effect.

Polysaccharides - have the ability to retain water, which gives the effect of immediate and long-term hydration. They reduce the unevenness of the surface of eyelashes and eyebrows, repair and smooth their structure.

Eyebright extract - herbal "compress", has a beneficial effect on the eye area. It soothes and moisturizes, reduces signs of fatigue, prevents irritation.

Peptides - cause the effect of longer, thicker and stronger eyelashes. The specially selected peptide - Biotinoyl Tripeptide-1 contained in the product strengthens the hair fibers, improving the condition of the eyelashes.

Pumpkin seed extract - strengthens eyelashes, preventing them from falling out.

 Indications: serum stimulating eyelash growth.

 How to use: On clean and dry skin of the upper eyelids (after removing make-up and washing with water), apply a small amount of the preparation with one stroke of the applicator (do not repeat) right at the base of the eyelashes (similar to eyeliner). Can be used on eyebrows. Apply once a day at night. In the event of the preparation coming into contact with the eyes, rinse with plenty of water. Use daily for 3-8 weeks, and then 2-4 times a week to maintain the effect.

 Main ingredients: Bimatoprost, biotin, panthenol, polysaccharides, firefly extract, peptides, pumpkin seed extract.

 Contraindications: The product contains bimatoprost. It should not be used by pregnant and breastfeeding women, people undergoing chemotherapy and under 18 years of age. Do not use in case of eye diseases or hypersensitivity to any component of the product. Avoid getting the preparation into the eyes.

The bimatoprost contained in the product may cause eye redness, itching, discomfort or dryness. In such cases, the use of the preparation should be discontinued for 5-7 days. If symptoms persist, consult a doctor. With prolonged use at the application site, the skin of the eyelids may darken. In most cases, the effect disappears after discontinuation of use.

BIOTEBAL LASHES XXL

Beautiful eye frame, thick, black and long lashes that do not fall out, but grow and allow you to get a unique look. Each of us dreams of such eyelashes, which is why we eagerly reach for the specifics from the pharmacy and store shelves. There is no shortage of products and we are able to choose one that will meet all our expectations. Among the available eyelash preparations, one of the most popular is Biotebal Lashes XXL. How does it work and what effects can you expect when using it?

A specialized serum with a unique formula

The unique formula of Biotebal Lashes XXL means that after just 3 weeks of use, you can count on the effect of long, beautiful and healthy eyelashes. The composition of the preparation includes several active ingredients that together create the Inno-BiBiotinTM formula.

One of the most important ingredients of the preparation is biotin, i.e. vitamin H, which helps to maintain healthy hair. Right next to it, there is bimatoprost, which inhibits the process of lash loss and stimulates their growth. It is one of the best-known ingredients with this effect in the world. Gives eyelashes a deep, dark color.

Biotebal Lashes XXL is the presence of a selected peptide - Biotinoyl Tripeptide-1. Eyelash loss is also prevented by pumpkin seed extract, while panthenol - provitamin B5, has a regenerating effect. Thanks to it, eyelashes are smoothed and thickened, as well as protected against damage. In addition, we know the well-known eyebright extract, which works well on the entire eye area. It reduces the visible signs of fatigue, soothes and moisturizes, and protects against irritation.

The last ingredient is polysaccharides responsible for the ability to retain water. The effect is perfect hydration of eyelashes, smoothing the structure and reducing unevenness.

EFFECTS AND APPLICATION OF BIOTEBAL LASHES XXL

Although the first effects of regular use can be noticed after just 3 weeks, the most spectacular ones may take up to 12 weeks, but not only the visual effects, but also the improvement of the condition of eyelashes or eyebrows, is worth the systematic use of the preparation.

The cosmetic is used daily for the first 3-8 weeks, and then 2-4 applications a week are enough to maintain the results already achieved.

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$18.89 - Estabiom Mama (formerly Estabiom Pregna), 20 capsules — Made in Poland — Free Delivery

$18.89 - Estabiom Mama (formerly Estabiom Pregna), 20 capsules — Made in Poland — Free Delivery
USP ZDROWIE #Health_in_pregnancy #Resistance #PREGNANCY_AND_MOTHERHOOD

Product description

Estabiom Mama is a dietary supplement in the form of capsules intended for women, especially during pregnancy and breastfeeding. The formula is a combination of three types of bacteria from the genus Lactobacillus, inulin and vitamin D in the form of cholecalciferol. One capsule contains 7.5 billion lactic acid bacteria, including the intestinal strain Lactobacillus rhamnosus GG and two strains of gynecological bacteria, 1000 IU of vitamin D and 100 mg of inulin. Vitamin D supports the proper functioning of the immune system and the maintenance of healthy bones and teeth. It also takes part in the process of cell division.

The bacterial strains in Estabiom Mama are resistant to stomach acids and digestive enzymes. In addition, the preparation is stable at room temperature and does not require refrigeration.

Application

Supplementing the diet with the active ingredients of the preparation, in particular during pregnancy, puerperium and breastfeeding.

Recommended intake

Adult women: 1 capsule daily.

The capsule can be swallowed whole or opened and its content dissolved in lukewarm liquid (eat immediately after preparation).

Ingredients

Inulin, capsule shell: hydroxypropylmethylcellulose, Lactobacillus rhamnosus GG (ATCC 53103), Lactobacillus acidophilus La-14, modified starch, sucrose, anti-caking agent: magnesium salts of fatty acids, dye: titanium dioxide, sodium triglyceride, anti-glycosyl chloride, anti-glycosylated chain , binding agent: silicon dioxide, antioxidant: alpha-tocopherol, vitamin D (cholecalciferol).

1 capsule contains:

vitamin D 25 µg (500%) *, Lactobacillus rhamnosus GG ATCC 53103 5 x 10 ^ 9 CFU **, Lactobacillus acidophilus La-14 2 x 10 ^ 9 CFU **, Lactobacillus rhamnosus HN001 0.5 x 10 ^ 9 CFU * *, inulin 100 mg.

* RWS - Reference Value of Consumption

** CFU - Colony-forming Unit

Warnings

Do not use if you are allergic to any of the ingredients of the product.

Important tips

Do not exceed the recommended daily dose.

A balanced diet and a proper lifestyle are important for the functioning of the human body.

A dietary supplement cannot be used as a substitute (replacement) for a varied diet.

Store in the original packaging, at room temperature, in a dry place, out of the reach of small children.

Protect from light.

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$68.24 - BIOXSINE SERUM AGAINST HAIR LOSS 6ML X 24 PCS — MADE IN GERMANY — FREE SHIPPING

$68.24 - BIOXSINE SERUM AGAINST HAIR LOSS 6ML X 24 PCS — MADE IN GERMANY — FREE SHIPPING
BIOTA LABORATORIES #For_hair #Hair_ampoules #COSMETICS

BIOXSINE HERBAL SERUM AGAINST HAIR LOSS 

Serum BIOXSINE herbal formula against hair loss was developed especially for people struggling with the problem of hair loss and / or people who want to strengthen their hair and give it elasticity.

Properties

• Effectively prevents hair loss
• Promotes the growth of new hair
• Strengthens active hair follicles
• It gives the hair volume and restores bounce
• The plant origin guarantees no side effects and ease of use
• Efficacy and safety confirmed in clinical trials (DERMATEST)
• It does not contain dyes and fragrances

Use:

Wash your hair with BIOXSINE shampoo and dry with a towel. Apply the BIOXSINE serum to damp and clean hair, starting at the point of hair loss and gradually cover the entire area covered with hair. With circular movements, gently massage the preparation with your fingertips for about a minute so that the skin absorbs the serum. Do not rinse.

3 phases of therapy:

Duration 48 days (1 ampoule every other day)

Duration 12 weeks (2 ampoules per week)

Duration 24 weeks (1 ampoule per week)

BIOXSINE serum can be used during the day or in the evening. However, it should be remembered that the preparation should remain on the hair for a minimum of 8 hours.

Components:

BAQUA, BIOCOMPLEX B11 (URTICA URENS & DIOICA EXTR. (NETTLE), CHAMOMILLA RECUTITA EXTR, ACHILLEA MILLEFOLIUM EXTR. (COMMON YARROW), CERATONIA SILIQUA EXTR. (CAROB), EQUISETUM ARVROENSE EXTR.

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$18.89 - Doppelherz Aktiv Magnesium + Potassium, 30 tablets — Made in Germany — Free Delivery

$18.89 - Doppelherz Aktiv Magnesium + Potassium, 30 tablets — Made in Germany — Free Delivery
QUEISSER PHARMA #Vitamins_and_minerals #Multivitamin #HEALTH_CARE

Product description

Doppelherz Aktiv Magnesium + Potassium is a special complex that helps to increase the energy capabilities of the body and maintains the balance of electrolytes at an optimal level, which has a positive effect on the activity of the cardiovascular, nervous and muscular systems.

Composition

magnesium - 300 mg

potassium - 300 mg

zinc - 5 mg

vitamin B6 4 mg

iron - 3.5 mg

chromium - 30 mcg

vitamin B12 - 2 μg

Indications for use

As an additional source of iron, magnesium, potassium, zinc, chromium, vitamins B6, B12. For the prevention of cardiovascular diseases. To prevent "chronic fatigue syndrome". Also, increasing efficiency when playing sports. In type II diabetes mellitus, to prevent complications of diabetes.

Mode of application

Adults and children over 14 years of age, take 2 tablets daily with meals. Duration of admission is 2-3 weeks. After a break of 1-2 months, repeated admission is possible.

Contraindications

With individual sensitivity to the components of the preparation.

Specifications

Product type: vitamin mineral complex

Purpose: additional source of magnesium, potassium

Release form: tablets

Quantity: 30 pcs

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$26.24 - Septogal + lactoferrin Strong 27 tablets — Made in Romania — Free Delivery

$26.24 - Septogal + lactoferrin Strong 27 tablets — Made in Romania — Free Delivery
Aesculap #Pain #Sore_throat #HEALTH_CARE

Product description

Dietary supplement Septogal + Lactoferin STRONG is intended for prophylaxis and as an adjuvant in acute bacterial, viral or fungal infections, namely pharyngitis, laryngitis, gingivitis, stomatitis. It helps to relieve the main unpleasant symptoms of such diseases - sore throat and sore throat, heaviness when swallowing, hoarseness of the voice. Has a quick effect, acts directly on the site of inflammation.

Active ingredients

Lozenges contain Lactoferrin, which is the most active glycoprotein in colostrum, plays an important role in the formation of immunity in the body, and is also involved in the supply and absorption of iron. Lactoferrin protects against microbes, viruses, fungi and has an anti-inflammatory effect on the entire respiratory tract. It has a disinfecting effect in the oral cavity and pharynx, reduces inflammation and oxidative processes at the level of mucous glands, has a calming effect, relieves pain and perspiration.

In addition, SEPTOGAL + Lactoferin STRONG contains Vitamin C, which is a powerful antioxidant and anti-inflammatory agent. Participates in the formation of collagen, which is necessary for the normal functioning of the gums and teeth. Vitamin C also contributes to the rapid healing of wounds after tooth extraction. Essential oils of menthol and eucalyptus have immunomodulatory, anti-inflammatory and antiviral effects, reduce edema, have local anesthetic and anti-irritant effects.

The presence of such a component as Methylene Blue in the composition of Septogal + Lactoferin STRONG ensures its action as an effective antiseptic with a disinfecting and redox effect.

The combination of components such as lactoferrin and essential oils has a powerful effect on breathing, so from the first minutes relief is felt not only in the throat, but also in the sinuses (helps with a stuffy nose).

The product is also indicated in dentistry: for postoperative restoration of the oral cavity, tooth extractions and after any dental intervention for prophylaxis and local anesthetics.

Septogal + STRONG lactoferrin is recommended even for patients with diabetes mellitus, since it does not contain sugar.

Indications for use

It can be recommended in dietary diets as an additional source of vitamin C, B vitamins, lactoferrin, to promote general strengthening of the body, normal functioning of the immune system, and support a healthy oral mucosa.

Septogal + STRONG lactoferrin is recommended as an adjuvant for:

• sore throat and sore throat; difficult swallowing;
• hoarseness of voice;
• infectious and inflammatory diseases of the oral cavity and pharynx (tonsillitis, pharyngitis, etc.)
• colds and flu;
• stomatitis, gingivitis and other diseases of the oral mucosa;
• dental interventions as an antiseptic and anesthetic.

Method of administration and dosage

Adults 2-3 tablets a day, dissolve in the mouth. The tablet should dissolve slowly in the mouth. After use, do not consume food or liquids for at least 30 minutes.

Application period: within 3-5 days.

Individual appointments and dosages as recommended by a doctor.

Without GMO.

Caution for use

In case of individual sensitivity to the components, as well as to women during pregnancy and lactation, you must first consult your doctor. Exceed the recommended amount for daily consumption.

Nutritional value per 100 g of product: proteins - 2.9 g; fats - 0; carbohydrates - 79.1.

Caloric content per 100 g of product: 328 kcal.

A dietary supplement cannot replace a complete and balanced diet. It is recommended to consult a doctor before use.

It is not a drug.

Compound

1 tablet (1000 mg) contains lactoferrin 30 mg, L-ascorbic acid (vitamin C) - 30.0 mg, menthol - 5.0 mg, eucalyptus essential oil (Eucaliptus globulus) - 4.0 mg, mint essential oil ( Mentha arvensis) - 2 mg, pine essential oil (Pinus sylvestris) - 2 mg, pyridoxine hydrochloride (vitamin B6) - 1.4 mg, riboflavin (vitamin B2) - 1.4 mg, thiamine hydrochloride (vitamin B1) - 1, 1 mg, stevia honey extract - 5.00 mg, methylene blue 0.5 mg, sorbitol, silicon dioxide, talc, magnesium stearate.

Storage conditions

Store in a dry, dark place and out of reach of children at a temperature not exceeding 25 ° C in the original packaging.

Shelf life - 2 years to give manufacturing. The expiration date is indicated on the packaging.

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$26.24 - CeraVe cleansing gel for face and body for normal to oily skin 236 ml — Made in France — Free Delivery

$26.24 - CeraVe cleansing gel for face and body for normal to oily skin 236 ml — Made in France — Free Delivery
Cosmetic Active Internationale #For_the_body #Bathing_and_washing_the_body #Shower_gels #COSMETICS

Product description

CeraVe® Intensive Cleansing Gel for oily skin deeply cleanses and refreshes the skin, removing excess sebum, impurities and makeup.

Does not damage the protective skin barrier.

Niacinamide soothes irritated skin.

Active ingredients

Ceramides (1, 3, 6-II), Hyaluronic acid, Niacinamide, Phytosphingosine, Cholesterol.

Mode of application

Lather the gel in the palms of your hands and apply to the skin in a circular motion. Wash off with plenty of water. Avoid eye area. In case of contact with eyes, rinse immediately with water.

Features of the

MVE technology - gradual release of active ingredients for long-term hydration;

For normal to dry skin of the face and body;

Hypoallergenic;

Paraben-free;

Fragrance-free;

Non-comedogenic - does not clog pores.

Structure

Aqua / water, cocamidopropyl hydroxysultaine, glycerin, sodium lauroyl sarcosinate, propanediol, peg-150 pentaerythrityl tetrastearate, niacinamide, peg-6 caprylic / capric glycerides, ceramide co np, ceramide ap, ceramide eop, carbomer, sodium tribute sodium chloride, sodium lauroyl lactylate, sodium hyaluronate, cholesterol, phenoxyethanol, disodium edta, citric acid, tetrasodium edta, phytosphingosine, xanthan gum, ethylhexylglycerin.

Storage conditions

Store at temperatures from + 6 ° C to + 25 ° C.

Expiration date - 36 months.

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$39.89 - Alpha D3-Teva 0.5 mcg 30 capsules — Made in Spain — Free Delivery

$39.89 - Alpha D3-Teva 0.5 mcg 30 capsules — Made in Spain — Free Delivery
TEVA #Vitamins_and_minerals #Vitamins #Vitamin_D #HEALTH_CARE

Pharmacological properties

Pharmacodynamics. Alpha d3-teva is a highly effective active metabolite of vitamin d3 that regulates calcium and phosphorus metabolism. Alfacalcidol (1-alpha hydrocholecalciferol) is rapidly converted to calcitriol (1,25-dihydrocholecalciferol, d-hormone) in the liver. Calcitriol is one of the main metabolites of cholecalciferol (vitamin d3) in maintaining calcium and phosphorus homeostasis. alpha d3-teva is transformed into 1,25-dihydrocholecalciferol (d-hormone) and thus increases its level in the blood. this causes an increase in the absorption of calcium and phosphorus in the intestine, an increase in their reabsorption in the kidneys, an increase in bone mineralization, and a decrease in the level of parathyroid hormone in the blood. in patients with age-related disorders of 1-alpha-hydroxylation in the kidneys, the intake of alpha-d3-teva contributes to the sufficient formation of calcitriol, which neutralizes the deficiency of d-hormone. Alpha d3-teva restores a positive calcium balance, as a result of which the intensity of bone resorption decreases, which helps to reduce the incidence of fractures. increases bone mineral density. With the course of use of the preparation, a decrease in the severity of bone and muscle pain associated with a violation of phosphorus-calcium metabolism is noted, coordination of movements and maintenance of balance improves, muscle strength increases, as a result of which the frequency of falls decreases.

Pharmacokinetics. After oral administration, Alpha D3-Teva is rapidly absorbed in the gastrointestinal tract. The time to reach Cmax of the preparation in blood plasma is 8-18 hours. The onset of action is after 6 hours, the duration of action is up to 48 hours.

In the liver, alfacalcidol is rapidly transformed into calcitriol (1,25-dihydrocholecalciferol, D-hormone). A smaller part of the preparation is transformed into bone tissue.

Unlike natural vitamin D3, the biotransformation of the preparation does not occur in the kidneys, which makes it possible to use it in patients with renal pathology.

Indications

Postmenopausal osteoporosis. osteoporosis associated with glucocorticoid treatment. softening of bones in old age (osteomalacia) as a result of insufficient absorption, for example, in the case of malabsorption and postgastrectomy syndrome. to significantly reduce the incidence of falls in the elderly. with hypoparathyroidism or hypophosphatemic (vitamin d-resistant) rickets / osteomalacia, additional therapy with alpha d3-teva may be indicated if the plasma calcium level is 2.2 mmol / l. diseases accompanied by impaired 1-alpha hydroxylation in the kidneys, which, in turn, cause disorders of vitamin d metabolism (for example, renal osteodystrophy with a decrease in calcium absorption and a plasma calcium level of 2.2 mmol / l (8.8 mg / 100 ml), which can occur as a result of impaired renal function without or with dialysis, as well as in the beginning with a condition after kidney transplantation).

Application

Inside. the capsule should be swallowed whole, washed down with plenty of water. the dose and duration of therapy are determined by the doctor individually and depend on the nature of the disease and the effectiveness of therapy. in some cases, the preparation is used throughout life.

Unless otherwise prescribed by a doctor, the initial dose for adults is 1 μg of alfacalcidol (4 capsules of 0.25 μg, or 2 capsules of 0.5 μg, or 1 capsule of 1 μg) daily. Patients with more severe bone disease are prescribed higher doses: 1-3 mcg of alfacalcidol (4-12 capsules of 0.25 mcg, or 2-6 capsules of 0.5 mcg, or 1-3 capsules of 1 mcg) daily.

Children over the age of 6 years with a body weight of ≥20 kg who can swallow a capsule - 1 μg / day (except in cases of renal osteodystrophy).

For patients with hypoparathyroidism, the dose should be reduced after reaching normal blood calcium levels (2.2–2.6 mmol / L; 8.8–10.4 mg / 100 ml), or when the product of plasma calcium • phosphate concentrations is 3.5-3.7 (mmol / l).

Alpha D3-Teva capsules 0.25 mcg. If the daily dose is 0.5 mcg of alfacalcidol, take 1 capsule in the morning and in the evening every day. If the daily dose is 1 mcg of alfacalcidol, take 2 capsules in the morning and in the evening every day.

Alpha D3-Teva capsules, 0.5 mcg. If the daily dose is 0.5 mcg, take 1 capsule daily in the evening. If the daily dose is 1-3 mcg of alfacalcidol (2-6 capsules of 0.5 mcg), it must be divided in half and taken one half in the morning and the other half in the evening.

Alpha D3-Teva capsules 1 mcg. If the daily dose is 1 mcg of alfacalcidol, take 1 capsule in the evening every day. If the daily dose is 3 mcg of alfacalcidol, take 1 capsule in the morning and 2 capsules of Alpha D3-Teva in the evening.

Contraindications

Hypersensitivity to alfacalcidol, peanuts, soy or any other components of the preparation; hypersensitivity to vitamin d and manifestations of vitamin d intoxication; plasma calcium level 2.6 mmol / l; the product of calcium concentrations • plasma phosphate 3.7 (mmol / l); alkalosis with a ph level of venous blood of 7.44 (lactate alkalosis syndrome, burnett syndrome); metastatic calcification; hypersensitivity to analogs of vitamin d.

Side effects

If the dose of alfacalcidol is not adjusted, an increase in the level of calcium in the blood is possible, which disappears when the dose is reduced or the preparation is temporarily discontinued. signs of a possible increase in blood calcium levels - fatigue, gastrointestinal disorders (vomiting, heartburn, abdominal pain, nausea, epigastric discomfort, constipation, diarrhea), anorexia, dry mouth, moderate muscle pain, bone pain, joints, weight loss, polyuria, increased sweating, headache, thirst, vertigo, increased levels of calcium and phosphate in the urine, nephrocalcinosis, hypersensitivity reactions, including pruritus, rashes, urticaria.

During therapy with alfacalcidol, adverse reactions may occur, which in frequency are defined as very often (≥1 / 10), often (≥1 / 100 to 1/10), infrequently (≥1 / 1000 to 1/100), rarely (≥ 1/10 000 to 1/1000), very rare (1/10 000), unknown (impossible to establish from the available data).

Often: hypercalcemia *, hypercalciuria.

Rarely: hyperphosphatemia, in order to prevent which the patient can be prescribed inhibitors of phosphate absorption (such as aluminum compounds); tachycardia, weakness, headache, dizziness, drowsiness.

Very rarely, including isolated cases: heterotopic calcification (cornea and blood vessels), which disappears after preparation withdrawal; a slight increase in HDL in blood plasma. In patients with severe renal impairment, hyperphosphatemia may develop; allergic skin reactions (itching) and anaphylactic shock, the latter can be caused by the peanut butter that is part of the preparation.

Unknown: hypersensitivity.

* Hypercalcemia is also associated with reactions such as hyperkaliuria, ectopic calcification, kidney and heart damage.

Special instructions

Alfacalcidol should not be administered to patients with hypercalcemia.

The preparation is prescribed with caution:

patients prone to hypercalcemia, especially with urolithiasis;

patients who are simultaneously using cardiac glycosides or digitalis preparations, since hypercalcemia can lead to arrhythmias in such patients.

During the period of use of the preparation, it is necessary to regularly (at least 1 time in 3 months) monitor the level of calcium in the blood plasma and urine, monitor the development of the therapeutic effect and, if necessary, adjust the dose of alfacalcidol in order to avoid the development of hypercalcemia and hypercalciuria. In the presence of biochemical signs of normalization of the bone structure (normalization of the ALP content in the blood plasma), a corresponding decrease in the dose of Alpha D3-Teva is necessary, which avoids the development of hypercalcemia. Hypercalcemia or hypercalciuria can be eliminated by discontinuing the preparation  and reducing calcium intake until its plasma concentration normalizes. Typically, this period is 1 week. Then therapy can be continued, starting at half of the last dose applied.

During therapy with alfacalcidol, plasma phosphate levels should be monitored to reduce the risk of ectopic calcification.

Adding vitamin D to the diet can be harmful to individuals who are already receiving adequate amounts of it from food and sunlight, since the difference between therapeutic and toxic concentration is very small.

Since alfacalcidol is the most active form of vitamin D, there is reason to expect the greatest risk of toxicity from its intake, however, its effects are quickly reversible if the intake is discontinued.

Alfacalcidol increases the absorption of calcium and phosphate in the intestine, therefore, in patients with renal insufficiency, their plasma concentrations should be monitored.

It is necessary to monitor the clinical manifestations of hypo- or hypercalcemia in elderly patients, especially in the presence of concomitant renal or cardiac pathology.

Early symptoms of hypercalcemia include polyuria; polydipsia; weakness, headache, nausea, constipation; dry mouth; muscle and bone pain; metallic taste in the mouth.

The medicinal product contains soybean oil. If the patient is allergic to peanuts or soy, the preparation is not recommended.

During pregnancy and breastfeeding. Although it has not been proven to have a negative effect on the fetus or infant, the preparation should not be used during pregnancy and lactation.

Due to the possible risk of developing persistent hypercalcemia, which can cause delayed physical and mental development, supravalvular aortic stenosis, retinopathy in infants, an overdose of a vitamin D analogue during pregnancy should be avoided.

The use of alfacalcidol during breastfeeding may increase the level of calcitriol in breast milk. Given this, the preparation is not used during breastfeeding.

Children. It is used in children over the age of 6 years with a body weight of ≥20 kg, who can swallow the capsule.

The ability to influence the reaction rate when driving or working with other mechanisms. The effect of the preparation on the ability to drive vehicles and work with complex mechanisms has not been identified, but the possibility of such adverse reactions as drowsiness and dizziness should be taken into account.

Interactions

In the treatment of osteoporosis, alpha d3-teva can be prescribed in combination with antiresorptive preparations of different groups and estrogens. the effect of alfacalcidol enhances the simultaneous use of estrogens in women during the pre- and postmenopausal period.

Vitamin D and its derivatives should not be used concomitantly with Alpha D3-Teva due to the possibility of additive interactions and an increased risk of hypercalcemia.

With the simultaneous use of Alpha D3-Teva with digitalis preparations, the risk of arrhythmia increases.

With simultaneous use with barbiturates, anticonvulsants (for example, carbamazepine, phenobarbital, phenytoin and primidone) and other preparations that activate enzymes of microsomal oxidation in the liver, it is necessary to take Alpha D3-Teva in a higher dose.

GCS can also reduce the effect of vitamin D.

The absorption of alfacalcidol is reduced when it is used with cholestyramine, colestipol, sucralfate, antacids with a high aluminum content. Alpha D3-Teva and aluminum-based antacids cannot be used simultaneously, the interval between doses should be at least 2 hours.

With the simultaneous use of Alpha D3-Teva and magnesium-based antacids, the risk of developing hypermagnesemia increases.

With the simultaneous use of calcium preparations, thiazide diuretics, the risk of developing hypercalcemia increases.

Rifampicin and isoniazid may reduce the effectiveness of vitamin D.

Overdose

With a single overdose (25-30 mcg) of alfacalcidol, no harm to health was detected. subsequent cases of alfacalcidol overdose may cause hypercalcemia.

Symptoms: anorexia, weakness, lethargy, dizziness, headache, nausea, dry mouth, constipation, diarrhea, heartburn, vomiting, abdominal pain, bone pain, increased sweating, drowsiness, itching, tachycardia. Perhaps the appearance of polyuria, polydipsia, nocturia, thirst, proteinuria with impaired renal function, weight loss.

Treatment: stop taking the preparation. Depending on the severity of hypercalcemia, you can follow a calcium-free or low-calcium diet, drink fluids, carry out dialysis, use loop diuretics, GCS and calcitonin. In acute overdose, a positive effect is possible with gastric lavage and / or the use of mineral oil (which helps to reduce absorption and increase excretion of the preparation in the feces). There are no specific antidotes for alfacalcidol.

Storage conditions

In a tightly closed container at a temperature not exceeding 25 ° C.

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$22.04 - Laferofly Broncho Kids syrup 125 ml — Made in Serbia — Free Delivery

$22.04 - Laferofly Broncho Kids syrup 125 ml — Made in Serbia — Free Delivery
ESENSA d.o.o #Child_health #Cough_for_children #CHILD

Product description

Laferofly Broncho Kids syrup facilitates expectoration and helps to regenerate damaged respiratory mucosa in children.

Recommended

In order to maintain the normal functional state of the mucous membranes of the respiratory tract during seasonal colds.

To reduce the viscosity of sputum, to facilitate its discharge.

For converting a dry non-productive cough into a wet productive cough.

Active ingredients

Ivy is a medicinal plant that contains saponins glycosides that enhance the secretion of bronchial glands, have expectorant, antispasmodic, anti-inflammatory and antimicrobial activity.

Composition

10 ml of syrup (12.5 T (g)) contains herbal extract.

Active ingredients: dry ivy leaf extract - 87.5 mg.

Excipients: purified water, sucrose, glycerin, honey; preservatives: sodium benzoate, citric acid, caramel color.

Mode of application

Apply internally using the measuring cap included.

Children aged 3 to 5 years - 2.5 ml of syrup once a day, from 5 to 12 years old - 2.5 ml 2 times a day, adults and children over 12 years old - 5 ml 2 times a day ...

The duration of use is 5-7 days.

Shake the bottle thoroughly before each use!

Warning

Hypersensitivity to product components, allergy to bee products. Do not use for children under 3 years of age, pregnant women, breastfeeding. Simultaneous use with antitussives is not recommended. Use with caution in patients with gastritis or gastric ulcer. Laferofly Broncho Kids syrup contains sucrose, which must be taken into account by patients with diabetes mellitus, as well as those who follow a low-calorie diet. The product should not be used as a food substitute.

Do not exceed the recommended daily dose.

Do not use after the expiry date stated on the packaging. Consult a physician before use.

It is not a drug.

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$15.74 - 2 x SEPTOLETE JUNIOR 18 LOZENGES — MADE IN SLOVENIA — FREE SHIPPIN

$15.74 - 2 x SEPTOLETE JUNIOR 18 LOZENGES — MADE IN SLOVENIA — FREE SHIPPIN
KRKA #Child_health #Sore_throat_in_children #CHILD

Indications

Recommended for local treatment of mild infections of the mouth and throat (pharyngitis, laryngitis, the initial period of inflammation of the palatine tonsils); for children over 4 years old.

Composition

1 tablet contains the active substance: 1.2 mg of cetylpyridinium chloride and excipients: liquid maltitol (dry weight), maltitol, mannitol, levomenthol, lemon oil, wild cherry flavor, natural red color (Cochineal, E 120), glycerol, castor oil, colloidal anhydrous silica, magnesium stearate, titanium dioxide (E 171), povidone, Capol 600.

Action

Disinfectant, bactericidal.

Dosage

The usual dose of Septolete Junior is:

- in children over 4 years of age: up to a maximum of 4 lozenges a day, and in children from 10 to 12 years of age: up to 6 lozenges a day. 1 lozenge should be sucked every 3 to 4 hours;

- in adults and children over 12 years of age, a maximum of 8 lozenges a day is recommended. 1 lozenge should be sucked every 2 to 3 hours.

Do not take the preparation immediately before or during food and at the same time with milk.

Contraindications

Hypersensitivity (allergy) to cetylpyridinium chloride or any of the other ingredients of this medicine, do not use in the case of wounds and erosions in the mouth, because cetylpyridinium chloride slows down the wound healing process.

Additional information

Before use, read the leaflet, which contains indications, contraindications, data on side effects, dosage and information on the use of the medicinal product, or consult your doctor or pharmacist, as each preparation used improperly is a threat to your life or health.

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$50.39 - Dr Irena Eris Face Zone, Black Mud Mask Face mask 50ml — Made in Poland — Free Delivery

$50.39 - Dr Irena Eris Face Zone, Black Mud Mask Face mask 50ml — Made in Poland — Free Delivery
Dr. Irena Eris #For_face #Face_masks #COSMETICS

Product description

Detoxifying and Revitalizing Black Mask is a harmonious combination of perfect cleansing and caring properties, restoring good condition and healthy appearance of the skin.

A mask based on natural Brazilian clay, perfectly cleanses the skin, removes toxins and all impurities. It causes gentle exfoliation, while absorbing dead skin cells and excess sebum. Effectively unblocks pores, accelerates the regeneration processes and significantly improves the smoothness of the skin (+ 58% *). The mask intensively oxygenates and stimulates microcirculation, which may be felt in the form of a delicate, pleasant tingling sensation. Natural ingredients, mineral salts and oligoelements contained in the formula moisturize and revitalize the skin, restoring its healthy appearance. A specially selected fragrance has a soothing and relaxing effect.

After using the mask, the skin is cleansed, matted and refreshed, ideally prepared for further care steps.

Directions for use:

Gently massage the mask on the skin of the face, avoiding the eye area, leave it for about 10 minutes, then rinse with warm water or a cotton swab soaked in tonic. Apply a suitable care cream. Use 1-2 times a week.

* In vivo test at the Dr Irena Eris Center for Science and Research.

Dermatologically tested. Keep out of the sun.

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$31.49 - HIRUDOID OINTMENT 100G - MADE IN GERMANY - FREE SHIPPING

$31.49 - HIRUDOID OINTMENT 100G - MADE IN GERMANY - FREE SHIPPING
STADA #Musculoskeletal_system #Contusions_and_bruises #HEALTH_CARE

Indications

Blunt injuries with or without hematomas, inflammation of the superficial veins, swelling, bruises.

Composition

100 g of the ointment contains: active substance: mucopolysaccharide polysulfate 0.3 g / 100 g, which corresponds to 25,000 U, and excipients: glycerol 85%, methyl 4-hydroxybenzoate, propyl, stearic acid, ointment base with lanolin alcohols, emulsifying cetosteryl alcohol, myristyl alcohol , isopropyl alcohol, potassium hydroxide, thymol, purified water.

Action

The preparation accelerates the dissolution of already existing small blood clots, as well as the disappearance of bruises and swelling, and has an analgesic effect.

Dosage

The drug should be applied 2 to 3 times a day to the affected areas or, if necessary, more often. Depending on the size of the treated area, it is usually sufficient to apply 3 to 5 cm of the ointment. In the case of painful inflammation, the ointment should be gently spread over the affected areas. The drug can be used as an ointment dressing. Treatment usually takes up to 10 days for blunt injuries, and 1 to 2 weeks for superficial vein inflammation. Hirudoid can also be used for phono and iontophoresis. During iontophoresis, the ointment is administered under the cathode.

Contraindications

Do not use in case of hypersensitivity to the ingredients of the preparation; on damaged skin, open wounds, mucous membranes and eyes.

Additional information

Before use, read the leaflet, which contains indications, contraindications, data on side effects, dosage and information on the use of the medicinal product, or consult your doctor or pharmacist, as each drug used improperly is a threat to your life or health.

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