Medicinal Products

PARACETAMOL PANPHARMA 10 mg / ml solution for infusion box of 10 vials (glass) 10 ml

Generic drug of the therapeutic class: Analgesics
active ingredients: Paracetamol
laboratory: Panpharma

Injection solution for IV infusion
All forms

Indication

PARACETAMOL PANPHARMA is indicated for the short-term treatment of moderate pain, particularly in the postoperative period and in the short-term treatment of fever, when the intravenous route is clinically justified by the urgency of treating pain. or hyperthermia and / or when other routes of administration are not possible.

Dosage PARACETAMOL PANPHARMA 10 mg / ml solution for infusion box of 10 vials (glass) of 10 ml

PARACETAMOL PANPHARMA is indicated for the short-term treatment of moderate pain, particularly in the postoperative period and in the short-term treatment of fever, when the intravenous route is clinically justified by the urgency of treating pain. or hyperthermia and / or when other routes of administration are not possible.

Against indications

PARACETAMOL PANPHARMA is contraindicated:

In case of hypersensitivity to paracetamol or propacetamol hydrochloride (paracetamol prodrug) or to any of the excipients.

· In case of severe hepatocellular insufficiency.

Side effects Paracetamol Panpharma

As with all drugs containing paracetamol, side reactions are rare
(> 1/10 000, <1/1000) or very rare (<1/10 000), they are described below:

System

Rare

Very rare

> 1/10 000, <1/1000

<1/10 000

General

Discomfort

Hypersensitivity reaction

Cardiovascular

hypotension

Hepatic

Elevation of liver transaminases

Platelets / blood

thrombocytopenia

leukopenia

neutropenia

Cases of pain and burning at the injection site have been reported that may be related to an initial infusion rate that is too fast, not necessarily disappearing after the decrease in flow rate.

Cases of erythema, flushing, pruritus and tachycardia have been reported.

Very rare cases of hypersensitivity reactions ranging from simple skin rash or urticaria to anaphylactic shock have been reported and require discontinuation of treatment.

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