Faropenem Sodium

Faropenem sodium is the active ingredient.It may contain inactive ingredients that vary depending on the specific formulation (check your medication label).

Treatment of communityacquired pneumonia

Treatment of acute bacterial exacerbations of chronic bronchitis

Treatment of skin and skin structure infections

Farozone 200mg Tab (Faropenem Sodium) is a carbapenem antibiotic. It works by inhibiting bacterial cell wall synthesis, leading to bacterial cell death. It's effective against a broad spectrum of Gram-positive and Gram-negative bacteria.

Store at controlled room temperature (20-25°C/68-77°F). Protect from moisture and light. Discard any unused portion after the expiration date.

Dosage and frequency will be determined by your doctor based on your condition and response to treatment.

Follow your doctor's instructions precisely regarding how and when to take the medication.

Typically administered intravenously or intramuscularly.

Injection site reactions (if administered intravenously or intramuscularly)

Rare but serious: Clostridium difficile-associated diarrhea, allergic reactions (including anaphylaxis)

Diarrhea

Nausea

Vomiting

Abdominal pain

Headache

Rash

Alcohol Consumption

The interaction between faropenem and alcohol is generally considered minimal but always best to avoid excessive alcohol consumption while taking antibiotics.



While Driving or operating Machinery

Drowsiness or dizziness are possible side effects. Avoid driving or operating machinery if affected.



Pregnant & Breastfeeding Women

Consult your doctor before taking this medication if you are pregnant, breastfeeding, or planning to become pregnant.



Children

Dosage needs to be determined by a physician based on the child's weight and condition.



Kidney

Dose adjustment may be necessary for patients with impaired kidney function.



Liver

Liver impairment may necessitate dose adjustment. Consult your doctor.

Consult your physician or pharmacist for detailed information and specific prescribing information.

Refer to the official drug monograph from the relevant regulatory authority in your country.