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Karmetadin of the tab. of p/o of 35 mg No. 60

Karmetadin of the tab. of p/o of 35 mg No. 60
Karmetadin of the tab. of p/o of 35 mg No. 60
Karmetadin of the tab. of p/o of 35 mg No. 60
Karmetadin of the tab. of p/o of 35 mg No. 60
Karmetadin of the tab. of p/o of 35 mg No. 60
$28.59
Tax $28.59
  • Stock: In Stock
  • Model: 184883

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Description

tablets Karmetadin are shown to adults for symptomatic treatment of stable stenocardia at insufficient efficiency or intolerance of anti-anginal medicaments of the first line.

Structure

Active ingredient: trimetazidina digadrokhlorid;

1 tablet supports a trimetazidin of dihydrochloride of 35 mg;

Excipients: calcium hydrophosphate anhydrous, silicon dioxide colloidal anhydrous, polyethylene oxide, povidone, xanthane gum, magnesium stearate;

Film cover: Opadry® II Brown 85G565010 (polyvinyl alcohol, talc, polyethyleneglycol, titan dioxide (E 171), lecithin (soy) ferrous oxide red (E 172)); magnesium stearate, glycerin.

Contraindication

  • Hypersensitivity to active ingredient or to any excipient.
  • Parkinson's disease, parkinsonism symptoms, a tremor, a syndrome of "uneasy legs" and other motive disorders concerning above-mentioned.
  • Heavy renal failure (clearance of creatinine <30 ml/min.).

Route of administration

One tablet of 35 mg of a trimetazidin two times a day at meal time.

Drug is used inside in the morning and in the evening.

After 3 months of treatment needs to estimate treatment outcome and in the absence of effect trimetazidin it is necessary to cancel.

Pregnant

Use is not recommended to

Feature of use

by

.

Drivers

With care.

Overdose

Amount of data on overdose trimetazidiny is limited to

. Symptomatic treatment.

Side effects

  • from digestive tract: pain in abdominal area of a stomach, diarrhea, dyspepsia, nausea and vomiting.
  • from skin and hypodermic fabric: rash, itching, urticaria.
  • General disturbances: asthenia.

Interaction

is not revealed by

Interaction with other medicines. In particular, trimetazidin it is possible to appoint in a combination with heparin, kaltsipariny, antagonists of vitamin K, peroral lipidosnizhayushchy drugs, aspirin, β-blockers, antagonists of calcium, foxglove medicaments (trimetazidin does not influence digoxin level in blood plasma).

Storage conditions

to Store

at a temperature not above 25 °C out of children's reach.

Expiration date - 3 years.

Specifications

Characteristics
Active ingredients Trimetazidin
Amount of active ingredient 35 mg
Applicant World Medicine
Code of automatic telephone exchange C01EB15 Trimetazidin
Interaction with food In time
Light sensitivity Not sensitive
Market status The branded generic
Origin Chemical
Prescription status According to the prescription
Primary packing blister
Producer UORLD OF MEDICINE ILACH SAN. BE TIDZH. A.SH.
Quantity in packing 60 tablets (2 blisters on 30 pieces)
Release form tablets for internal use
Route of administration Oral
Sign Import
Storage temperature from 5 °C to 30 °C
Trade name Karmetadin