COMPOSITION: Each coated tablet contains Paracetamol 500 mg, Excipients.

INDICATIONS: Paracetamol is an effective analgesic and antipyretic for the control of mild or moderate pain caused by joint disorders, ear pain, headaches, odontogenic pain, neuralgia, minor surgical procedures, etc.

It is also effective for the treatment of fever such as that caused by viral infections, post-vaccination fever, etc.

DOSE: Adults: The usual dose for analgesia and fever control is 325 to 1,000 mg every four hours, up to a maximum of 4 grams per day.

In patients with renal insufficiency, it is recommended to increase the administration interval to six hours, as in patients with moderate renal damage, and to eight hours in patients whose glomerular filtration rate is less than 10ml/min.

In case of hepatic insufficiency, 2g/24 hours will not be exceeded and the minimum interval between doses will be 8 hours.

Pregnancy and Lactation: Corresponds to pregnancy risk category B, its non-prolonged use is considered safe during the three trimesters of pregnancy.

It is compatible with lactation.

CONTRAINDICATIONS and PRECAUTIONS:

Hypersensitivity to acetaminophen, because it is metabolized in the liver, it should be administered with caution in patients with liver damage, as well as in those who are receiving hepatotoxic drugs or who have some type of nephropathy.

The risk of hepatotoxicity is rather high in patients with alcohol dependence and in patients receiving more than one medication containing acetaminophen.

Avoid the use of high doses in patients with hepatic dysfunction.

Avoid use in patients with phenylketonuria or G6PD deficiency.

Use with caution in patients with dehydration or chronic malnutrition. Self-medication with paracetamol should be limited when being treated with anticonvulsants, since it enhances hepatoxicity and decreases the bioavailability of paracetamol.

COMPOSITION: Each coated tablet contains:

Calcium 400 mg, Iron 18 mg, Vitamin D 10 µg, Folic Acid 400 µg.

INDICATIONS: Flexa® NATAL FORTE in combination with regular exercise and a balanced diet with sufficient calcium helps women, especially pregnant women, to maintain good bone health, contributes to normal bone maintenance, with adequate intakes of folic acid, can reduce the risk a woman from having a child with a spinal or brain defect, in combination with a diet rich in iron, promotes normal development and cognitive function, with an adequate supply of oxygen, in addition to normal cell division.

This food is a source of: Calcium, Vitamin D, Folic Acid and Iron.

DOSE: Pregnant women and lactating women are recommended to take one tablet with breakfast.

CONTRAINDICATIONS and PRECAUTIONS:

This product is not suitable to be consumed as the only food source.

Do not exceed the recommended dose.

If you are taking any medication, consult your doctor before taking this product.

COMPOSITION:

Amount per dose (mg / 5 mL):

Micronized Ibuprofen ……………………………… 200,000

Amount (mg / 100 mL):

Micronized Ibuprofen ……………………………… 4000,000

THERAPEUTIC CLASSIFICATION: NSAIDs, non-selective inhibitor of cyclooxygenase.

PROPERTIES:

Ibuprofen is a non-steroidal compound derived from propionic acid with marked anti-inflammatory, analgesic, and antipyretic properties. Its mechanism of action is based on the inhibition of prostaglandin synthesis. Prostaglandins play an essential role in the onset of fever, pain and inflammation. Experimental data suggest that ibuprofen can competitively inhibit the effect of low doses of acetylsalicylic acid on platelet aggregation when administered concomitantly.

INDICATIONS:

• This medicine is indicated in children from 7 years old.

• Symptomatic relief of occasional mild or moderate pain.

• Febrile states.

DOSAGE AND ADMINISTRATION:

Orally. The recommended dose is:

Pediatric population

The dose of ibuprofen to be administered depends on the age and weight of the child. As a rule, the recommended daily dose is 20 to 30 mg / kg of weight, divided into three or four individual doses. As an orientation, the following dosage regimen is recommended:

- Children of 25 to 40 kg of weight (7-12 years approximately): The recommended daily dose is 600 – 800 mg of ibuprofen, divided into 3 or 4 doses (1 on 3 or 4 times a day), the dose being recommended daily maximum 800 mg. – Children over 40 kg and adolescents (over 12 years): The recommended daily dose is 800 -1,200 mg of ibuprofen per day, divided into 3 or 4 doses (1-2 envelopes 3 or 4 times a day ), with a maximum recommended daily dose of 1,200 mg. The use of other presentations with more adequate doses for treatment in adolescents and adults is recommended. The interval between doses will depend on the evolution of the symptoms, but it will never be less than 4 hours.

CONTRAINDICATIONS:

This medicine is contraindicated:

- In patients with hypersensitivity to ibuprofen, to other NSAIDs or to any of the excipients included in the section

- In patients who have experienced asthma attacks, acute rhinitis, urticaria, angioneurotic edema or other allergic-type reactions after using substances with similar action (eg acetylsalicylic acid or other NSAIDs).

- In patients with a history of gastrointestinal hemorrhage or perforation related to previous treatments with NSAIDs. Peptic ulcer / active or recurrent gastrointestinal hemorrhage (two or more different episodes of proven ulceration or bleeding),

- In patients with severe heart failure (NYHA class IV).

- In patients with severe renal dysfunction.

- In patients with severe hepatic dysfunction.

- In patients with hemorrhagic diathesis or other coagulation disorders.

- During the last trimester of pregnancy

WARNING AND PRECAUTIONS:

Gastrointestinal Risks: Gastrointestinal Hemorrhages, Ulcers and Punctures: During treatment with nonsteroidal anti-inflammatory drugs (NSAIDs), including ibuprofen, gastrointestinal hemorrhages, ulcers and perforations have been reported. Cardiovascular and cerebrovascular risks: Special caution should be exercised in patients with a history of hypertension and / or heart failure, since fluid retention and edema have been reported in association with NSAID treatment. Risks of severe skin reactions: Severe skin reactions, some fatal, including exfoliative dermatitis, Stevens-Johnson syndrome, and toxic epidermal necrolysis have been reported with very rare frequency in association with the use of NSAIDs. Renal and / or hepatic insufficiency: Ibuprofen should be used with caution in patients with liver or kidney disease and especially during the simultaneous treatment with diuretics, since it should be taken into account that the inhibition of prostaglandin synthesis can cause fluid retention and deterioration of renal function.

PREGNANCY AND LACTATION: contraindicated its use, The inhibition of prostaglandin synthesis, can negatively affect the pregnancy and / or the development of the embryo / fetus

OVERHEADING:

Symptoms due to overdose include: vertigo, spasms, hypotension or depression of the nervous system (reduction of consciousness). If less than one hour has elapsed, a gastric lavage is recommended. The oral intake of substances such as activated charcoal to reduce drug absorption is also considered beneficial. If more than one hour had elapsed, due to the acid nature of the medication, the alkalinization of urine and diuresis is recommended to favor its elimination. In case of intoxication, metabolic acidosis can occur.

REGISTERED PRESENTATIONS:

Box x 1 bottle x 120mL oral suspension + dosing syringe + insert

Venous Health – Venotonic – Vasculoprotective – Tired, swollen and achy legs

VENOSTASIN BENEFITS:

3 presentations, one for each patient’s need.

Venostasin Gel for direct application on the legs, giving a gentle circular massage from the ankles up to the hips. Apply Venostasin Gel 2 times a day.

Venostasin retard capsules, 2 doses a day

Venostasin Tablets 3 doses a day.

Venostasin has a double antiedematous action, increases capillary resistance and decreases capillary permeability, due to the sealing effect of the endothelium.

Venostasin has phlebotonic action, decreases the concentration of lysosomal enzymes increased in patients with varicose veins.

Venostasin provides the patient with a hemodynamic action, due to the fact that it increases the speed of blood flow and decreases blood viscosity.

Venostasin increases venous tone, favoring the return of blood from the periphery to the heart, reducing venous stasis.

Venostasin, due to its venotonic and vasculoprotective effect, acts favorably on the signs of symptoms of heaviness, fatigue, pain, cramps, varicose veins, edema and chronic venous disease.

Venostasin can be used for a long time.

INDICATIONS:

VENOSTASIN RETARD CAPSULES AND VENOSTASIN TABLETS: Varicose veins. Varicose syndrome. Chronic venous insufficiency and its manifestations: edema (swelling), night cramps, pain, burning, heavy legs, itching, trophic disorders due to capillary fragility.

VENOSTASIN GEL: For the local treatment of varicose syndrome, phlebitis, thrombophlebitis and edema. In general, occupational and sports medicine for the treatment of bruises, bruises, sprains, dislocations and tendinitis.

COMPOSITION

• Venostasin Retard Capsules Horse Chestnut Extract (Equivalent to Escin 50Mg) 300mg

• Venostasin Tablets ß Escin 15mg Cas N° (6805-41-0)

• Venostasin Gel – Each 100gr of gel contains: ß Escin 1g – Ethinyl Glycolic MonoSalicylic Acid Ester 5g – Sodium Heparin 5,000UI

MECHANISM OF ACTION:

Double anti-edematous action: Since it increases capillary resistance and decreases capillary permeability due to the “sealing” effect of the endothelium.

Phlebotonic action: Since it decreases the concentration of lysosomal enzymes (which are increased in patients with varicose veins) and that destroy the proteoglycans of the venocapillary wall.

Hemodynamic action: Since it increases the speed of venous flow and decreases blood viscosity.

DOSAGE:

Venostasin Gel. Apply 2 times a day, give a gentle massage from the ankle, going up to the hips.

Venostasin Capsules Retard. Take one capsule after breakfast and dinner.

Venostasin Tablets. Take one tablet every 8 hours.

CONTRAINDICATIONS: None known – Hypersensitivity to horse chestnut.

SIDE EFFECTS: Occasionally mild epigastric discomfort may occur, in such cases take the capsules with food.

INTERACTIONS: They have not been reported to date.

PRECAUTIONS FOR USE: In case of unsatisfactory or inadequate response, after six weeks, you should consult your doctor to rule out other probable causes of edema.

Do not use in children, pregnancy and lactation.

**If symptoms persist consult your MD

COMPOSITION: 10 g (about 2 teaspoons) of DALIVIT R jelly contains 3000 IU of Vitamin A, 0.75 mg Vitamin B1, 0.90 mg of Vitamin B2, 1.25 mg of B6, 40 mg of vitamin C, 200 IU of Vitamin D3, 7.5 IU of vitamin E, and 10 mg of nicotinamide, excipients cs.

ACTIONS AND CLINICAL PHARMACOLOGY: DALIVIT jelly contains the daily required amounts of Vitamin A, essential for growth and development, for the maintenance of epithelial tissue and vision. Vitamins B1, B2 and B6 are essential for the use of food and energy involved in the metabolism of carbohydrates, amino acids and fats in the formation of hemoglobin, and modulates neuromuscular transmission, Nicotinamide, which acts on the electron transfer reactions in the respiratory chain and prevents pellagra, Vitamin C, essential for the synthesis of collagen and intercellular material and prevents scurvy. Vitamin D3 is essential for proper regulation of calcium and phosphorus and bone mineralization. Vitamin E that prevents oxidation of fatty acids and reacts with free radicals, which are the cause of the damage of cell membranes.

INDICATIONS: Treatment and prevention of conditions resulting from the specific weakness of each component of DALIVIT R. Nutritional supplement for the whole family, especially children, that helps them grow with vitality, keeps them healthy and prevents disease. This nutritional supplement is effective during pregnancy and lactation.

DOSAGE: Children and infants: ½ teaspoon 2 to 3 times a day. School children, adolescents and adults: 1 teaspoon 2 times a day.

COMPOSITION: Each pill contains: 15 mg of vitamin B1, 3 mg vitamin B2, 15 mg of nicotinamide, 5 mg of vitamin B6, 10 mg of calcium pantothenate, and excipients c.s.p ad 1 tablet. SYRUP Each 5 mL contains: Vitamin B1: 1.5 mg, Vitamin B2: 0.6 mg, nicotinamide 10 mg, vitamin B12: 0.002 mg, biotin o.10 mg, folic acid: 0.14 mg.

INDICATIONS: Treatment and prevention of conditions resulting from the specific weakness of each component of complex B (beri-beri, ariboflavinosis, neuropathies induced by drugs or alcohol, pellagra, megaloblastic anemia, prevention of tube defects in pregnant women). Vitamin deficiency resulting from poor diet, by an increase in requirements such as pregnancy and lactation, or induced by drugs or disease.

DOSAGE: Adults and children over 12 years: 2 to 3 pills a day or 2 teaspoons (10 mL) of syrup with every meal. Children: 1 teaspoon (5 mL) 2 times daily with meals.

Quantity 100 g of cream contains:

Ketoconazol…………………… 2 g

Excipiente c.s.p……….… 100 g

INDICATIONS: Superficial fungal infections: cutaneous candidiasis, pityriasis versicolor, seborrheic dermatitis, ringworm of the body, groin, hands and feet.

DOSAGE: Apply 1 or 2 times a day, the recommended duration of the treatment is:

He had a body: 3-4 weeks.

Ringworm of the feet and hands: 4-6 weeks

Jock itch and seborrheic dermatitis: 2-4 weeks

Cutaneous candidiasis and Pityriasis versicolor: 2-3 weeks

HOW TO USE: This medication is for topical (cutaneous) use, apply in sufficient quantity on and around the affected areas.

PRECAUTIONS FOR USE: For external use only. It should not be used for ophthalmic treatments. Avoid contact with eyes. This medication may cause local skin reactions (such as contact dermatitis) because it contains propylene glycol, cetyl alcohol, and stearyl alcohol.

CONTRAINDICATIONS: In people who have been shown to be hypersensitive to ketoconazole or any of the excipients

“IF SYMPTOMS PERSIST, CONSULT YOUR DOCTOR”