Recorded active ingredients: Diphenhydramine
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These listings match the full ingredient set recorded for димедрол 1% для инъекций. Strength, dosage form and route may differ or be missing. This does not establish interchangeability; confirm a suitable product with a pharmacist.
Long-term or too frequent administration of the drug in young children can lead to inhibiting of the central nervous system, hypothermia, coma, and prolonged expansion of the pupil. Nafazolin can cause a sudden decrease in blood pressure and tachycardia.
There is no data regarding the acute overdose of drops injected locally into the conjunctival bag.
Hypersensitivity.
Sonnness, dry mouth, dizziness, nausea, headache, weakness, numbness of the mucous, decrease in reaction rate.
Drowsiness, dizziness, decreased reaction rate, headache, weakness, dry mouth, numbness of the mucous, nausea.
Increased excitability (especially in children).
Allergic diseases, allergodermatosis, peptic ulcer of the stomach and duodenum, insomnia, vomiting of pregnant women, Meniere syndrome, seasickness, radiation sickness, parkinsonism.
Allergic diseases, allergodermatosis, peptic ulcer of the stomach and duodenum, insomnia, vomiting of pregnant women, Meniere syndrome, seasickness, radiation sickness, parkinsonism.
Allergic reactions of the upper respiratory tract (pump, lacrimation, perm in the throat or nose), colds.
Keep out of the reach of children.
The shelf life of the drug Dimedrol is 1% for injection4 years.Do not apply after the expiration date indicated on the package.
1 ampoule with 1 ml of injection solution contains diphenhydramine 10 mg; in a box of 10 pcs.complete with ampulse knife.
V / m. 1–5 ml, per day no more than 15 ml.