Pruf-P Tablet (Flupirtine 100mg / Paracetamol 325mg)

Pruf-P Tablet

Pruf-P  drug helps in treating pain caused due to menstrual cramps, tension headache, cancer, trauma, surgeries. Avoid using this drug if you are using it with other medicines. These medications may lead to liver injury and if you are allergic to any ingredient contained within this drug.

The dosage for this medication should be determined by the doctor based on your medical history and current condition. The usual dose is either 100 or 200 mg per day depending on the severity of the condition.

Take exactly as directed (do not increase dose or frequency); most adverse effects are related to excessive use. Take with food or milk. While using this medication, avoid alcohol and other prescription or OTC medications that contain acetaminophen.

Maintain adequate hydration (2-3 L/day of fluids unless instructed to restrict fluid intake). This medication will not reduce inflammation; consult prescriber for anti-inflammatory, if needed.

Report unusual bleeding (stool, mouth, urine) or bruising; unusual fatigue and weakness; change in elimination patterns; or change in color of urine or stool.

Information given here is based on the salt content of the medicine. Uses and effects of the medicine may vary from person to person. It is advisable to consult a Internal Medicine Specialist before using this medicine.

Use of Pruf-P 

This drug can be used in following conditions

Pain Relief

Side Effects

This drug may cause following side effects

Nausea Or Vomiting

Dizziness

Itching Or Rash

Abdominal Pain

Bloating

Tremor

Dryness In Mouth

Fatigue

Dosage

Are there any missed dose instructions?

Take the missed dose as soon as you remember. Skip the missed dose if it is time for the next scheduled dose.
Are there any overdose instructions?

Doctor consultation is advised if an overdose is suspected.

Work

This drug is an analgesic which works by upregulating Bcl-2, increasing glutathione level, activating an important potassium channel, and delaying calcium retention capacity loss of inter-mitochondrial membrane. It also acts as an NMDA receptor antagonist without binding to the receptor.