Таблетки OCSAAR PLUS

PATIENT PACKAGE INSERT IN ACCORDANCE WITH THE PHARMACISTS' REGULATIONS (MEDICINAL PREPARATIONS) - 1986

The dispensing of this medicine requires a doctor's prescription

Read the package insert carefully in its entirety before using this medicine

OCSAAR PLUS

Tablets

COMPOSITION

Each tablet contains: Losartan potassium 50 mg Hydrochlorothiazide 12.5 mg

Терапевтическая активность
Для лечения артериальной гипертензии.

THERAPEUTIC ACTIVITY

For the treatment of hypertension .

WHEN SHOULD THE PREPARATION NOT BE USED?

Do not use this medicine if you are pregnant or breastfeeding. Do not use this medicine if you are sensitive to any of its ingredients, including sulfonamide-derived drugs (consult your doctor about sulfonamide- derived drugs).

Do not use this medicine if you suffer from anuria.

Do not take this medicine without consulting a doctor before starting treatment [if you are suffering, or have suffered in the past, from impaired function of the respiratory system (e.g., asthma), the liver, the kidney/ urinary tract, or the thyroid gland, or if you are suffering now from diabetes, gout, lupus erythematosus, hyperlipidemia (high levels of cholesterol and triglycerides), and in cases of increased loss of fluids (diarrhea or vomiting).

HOW WILL THIS MEDICINE AFFECT YOUR DAILY LIFE?

Do not drink wine or alcoholic beverages while under treatment with this medicine.

WARNINGS

During treatment with this medicine, tests should be performed for blood and urine (including electrolytes).

If you are sensitive to any type of food or medicine, inform your doctor before commencing treatment with this medicine.

Discontinue treatment with this medicine before you undergo a test for parathyroid function.

If you are about to undergo surgery that requires anesthesia, even at the dentist's office, inform the attending doctor as there may be a sudden fall in blood pressure associated with the anesthesia.

Please inform your doctor if you suffer from dizziness during the first days of treatment with Ocsaar Plus.

Reduced amount of drinking, excessive perspiration, diarrhea or vomiting may

cause a fall in blood pressure, and possible syncope.

Kidney function test should be performed at the beginning of treatment.

DRUG INTERACTIONS

If you are taking another drug concomitantly, including a nonprescription drug, or if you have just finished treatment with another medicine, inform the attending doctor in order to prevent hazards or lack of efficacy arising from drug interactions. This is especially important for medicines belonging to the following groups: drugs affecting the central nervous system (e.g., tranquillisers, hypnotics, narcotics, analgesics, antidepressants including lithjum); other antihypertensives; antidiabetics; other diuretics; medicines which cause elevation of potassium blood levels, potassium supplement medications,

salt substitutes containing potassium; steroids; non-steroidal anti-inflammatory agents; medicines derived from resins to lower cholesterol (cholestyramine and colestipol); muscle relaxants; drugs which may cause a rise in blood pressure such as adrenaline.

SIDE EFFECTS

In addition to the desired effect of the medicine, adverse reactions may occur during the course of taking this medicine, such as dizziness, skin rash, back pain, edema, palpitation, sinusitis. These side effects usually disappear within a short time following the period of adaptation to the medicine. Side Effects that require special attention

Allergic reaction involving swelling of the face, lips, throat and/or tongue (rare): stop treatment and refer to your doctor immediately. If a syncope occurs, stop treatment and refer to your doctor immediately. In the event that you experience side effects not mentioned in this

leaflet, or if there is a change in your general health, consult your doctor immediately.

ADMINISTRATION AND DOSAGE

Dosage is according to doctor's instructions only. Do not exceed the recommended dosage.

This medicine is not intended for administration to children and infants.

Since this medicine is to be taken once daily, it is recommended that the tablet be taken at the same time every day.

If you forget to take this medicine at the specified time, take the missed dose as soon as you remember, but never take a double dose!

DIRECTIONS FOR USE

Do nqt chew! Swallow the tablet with a small amount of water, without regard to meals.

I "HOW- CAN" "YOU- ODN TRIBUTE" ~TO IF HE-SU CCESS-OF ~~THE~|

I TREATMENT?

Complete the full course of treatment as instructed by the doctor.

Even if there is an improvement in your health, do not discontinue use of this

medicine before consulting your doctor.

AVOID POISONING!

This medicine, and all other medicines, must be stored in a safe place out of the reach of children and/or infants, in order to avoid poisonina. If you have taken an overdose, or if a child has accidentally swallowed the medicine, proceed immediately to a hospital emergency room and bring the package of the medicine with you.

Do not induce vomiting unless explicitly instructed to do so by a doctor! This medicine has been prescribed for the treatment of your ailment; in another patient it may cause harm. Do not give this medicine to your relatives, neighbors or acquaintances.

Do not take medicines in the dark! Check the label and the dose each time you take your medicine. Wear glasses if you need them.

STORAGE

Store this medicine in a cool and dry place.

Even if kept in their original container and stored as recommended, medicines may be kept for a limited period onfy. Please note the expiry date of the medicine! In case of doubt, consult the pharmacist who dispensed the medicine to you. Do not store different medications in the same package.

Drug Reg. No.: 1112329411

Manufactured by Merck Sharp & Dohme B.V., Haarlem, Netherlands for Merck Sharp & Dohme (Israel - 1996) Company Ltd., P.O.Box 7121 Petah-Tikva 49170.