TRICORTIN

Indications for use

- polymyalgic neurosis syndrome

Directions for use and doses

2 ml is administered intramuscularly once a day as prescribed by the doctor.

Side effects

There have been no reported side effects that could be attributed to this drug.


Overdose

No overdose symptoms were reported.

Contraindications

- hypersensitivity to the components of the drug or other substances,

similar in chemical structure

- children and adolescents up to 18 years of age

Drug interactions

There have been no reports of interactions with other drugs.
There are no known cases of incompatibility of TRICORTIN® with other drugs.




Special instructions

Pregnancy and lactation

The drug can be administered during pregnancy and lactation under the direct supervision of a physician.

Features of the drug's influence on the ability to drive a vehicle or potentially dangerous machinery

The drug does not affect the ability to drive a car or operate machinery.

Release form and packaging

2 ml in orange glass ampoules type I, with a breaking point.

5 ampoules per blister pack made of polyvinyl chloride film.

1 blister pack together with instructions for medical use in the state and Russian languages ​​are placed in a cardboard box.

Storage conditions

Store at a temperature not exceeding 25°C

Keep out of the reach of children!



Shelf life

2 years

Do not use after the expiration date!



Conditions for dispensing from pharmacies

On prescription



Manufacturer/Packager

Fidia Pharmaceutisi S.P.A.,

35031, Abano Terme, Via Ponte della Fabbrica, 3/A, Italy




Registration Certificate Holder

Fidia Pharmaceutisi S.P.A.,

35031, Abano Terme, Via Ponte della Fabbrica, 3/A, Italy