Tempalgin coated tablets,

Tempalgin tab.

p / o captivity.

No. 100

Name ENG

TEMPALGIN

Clinical and pharmacological group

Analgesic-antipyretic combined composition

ATX code

Metamizole sodium in combination with psycholeptics

Dosage

500mg + 20mg

Structure

Active ingredients: metamizole sodium 500 mg

triacetonamine 4-toluenesulfonate (tempidone) 20 mg. Excipients: wheat starch, microcrystalline cellulose, talc, magnesium stearate, crospovidone (Kollidon K25), titanium dioxide, polyethylene glycol 400, castor oil, glycerol, dibudcylphthalate, 5 L dye green.

Indications

Moderate or mild pain syndrome (including headache, migraine, toothache, neuralgia, radicular syndrome, myalgia, arthralgia, algomenorrhea), especially in patients with increased nervous excitability

- mild pain of visceral origin (including renal, hepatic, intestinal colic) in combination with antispasmodic therapy

- pain syndrome after surgical and diagnostic interventions (as an adjuvant)

- an increase in body temperature with colds and other infectious and inflammatory diseases.

INN / Active ingredient

Metamizole sodium, triacetonamine-4-toluenesulfonate

Contraindications

Severe liver failure - severe renal failure - chronic heart failure - arterial hypotension (decrease in systolic blood pressure below 100 mm Hg) - oppression of hematopoiesis (granulocytopenia, leukopenia, agranulocytosis, cytostatic or infectious neutropenia) - deficiency of glucose-6-phosphate dehydrogenase - aspirin" asthma - pregnancy - lactation period (breastfeeding) - children's age (up to 14 years old) - hypersensitivity to metamizole sodium, pyrazolone derivatives or triacetonamine-4-toluenesulfonate. It is prescribed with caution in case of kidney diseases (pyelonephritis, glomerulonephritis, including history), hepatic / renal failure of moderate severity, with bronchial asthma, predisposition to the development of arterial hypotension,with prolonged alcohol abuse.

Storage conditions and periods

In a dry place, at a temperature not exceeding 25 degrees.

Expiration date: 4 years

Specifications

Category

Pain and fever

Scope of the drug

General

Release form

Tablet

Manufacturer country

Bulgaria

Package quantity, pcs

one hundred

Scope of application

Dentistry

,

Surgery

Minimum age from

14 years old

Way of introduction

Through the mouth

Vacation conditions

Without recipe

Brand name

Sopharma

The amount of the dosage form in the primary package

10 pieces.

Primary packaging type

Blister

Type of consumer packaging

Pack of cardboard

Dosage form

Film-coated tablets

Expiration date in days

1461

The target audience

Children

Package weight, g

ten

Mode of application

:

The tablets are taken orally, without chewing, with a sufficient amount of liquid, during or after meals. < br> Adults are prescribed 1 tablet 1-3 times / day, with insufficient effectiveness, you can take another 1 tablet.

< br> The maximum single dose is 2 tablets, the maximum daily dose is 6 tablets.

< br> Duration of admission - no more than 5 days.

< br> Increasing the daily dose or increasing the duration of treatment is possible only under the supervision of a doctor.

Pharmaco-therapeutic group

:

Combined analgesic (non-narcotic analgesic + anxiolytic)

Anatomical and therapeutic characteristics

:

N02BB72 Metamizole sodium, in combination with psychotropic drugs

Dosage (volume) of the substance in the preparation

:

Metamizole sodium 500 mg, triacetonamine 4-toluenesulfonate (tempidone) 20 mg

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