Inpen
Generic Name
Imipenem and Cilastatin
Manufacturer
Example Pharmaceutical Co. Ltd.
Country
Bangladesh
Loading images...
Price Details
Current market pricing information
Variant | Unit Price | Strip Price |
---|---|---|
inpen 1 gm injection | ৳ 1,300.00 | N/A |
Description
Overview of the medicine
Inpen is a broad-spectrum antibiotic containing Imipenem and Cilastatin. Imipenem is a carbapenem antibiotic effective against a wide range of bacteria, and Cilastatin prevents its breakdown in the kidneys, enhancing its effectiveness and reducing potential renal toxicity.
Uses & Indications
Dosage
Adults
Usually 250 mg to 1000 mg (Imipenem/Cilastatin) every 6 to 8 hours by IV infusion, depending on the severity and type of infection. Maximum daily dose is 4 gm.
Elderly
Dosage should be adjusted based on renal function, similar to adult patients with renal impairment.
Renal_impairment
Significant dosage reduction is required based on creatinine clearance (CrCl). Consult a dosing chart specific to CrCl levels.
How to Take
For intravenous infusion only. Reconstitute the powder with an appropriate diluent (e.g., 0.9% sodium chloride, 5% dextrose in water) and administer slowly over the recommended period.
Mechanism of Action
Imipenem inhibits bacterial cell wall synthesis by binding to penicillin-binding proteins (PBPs), leading to bacterial cell lysis and death. Cilastatin inhibits dehydropeptidase-I, an enzyme found in the renal tubules that metabolizes imipenem, thereby increasing the urinary concentrations of imipenem.
Pharmacokinetics
Onset
Rapid, with peak plasma concentrations occurring within 20 minutes after a 30-minute IV infusion.
Excretion
Primarily renal; approximately 70% of both imipenem and cilastatin are recovered in the urine within 10 hours after a 30-minute IV infusion.
Half life
Imipenem: approximately 1 hour; Cilastatin: approximately 1 hour.
Absorption
Administered intravenously, providing 100% bioavailability.
Metabolism
Imipenem is partially metabolized by renal dehydropeptidase-I (inhibited by cilastatin). Cilastatin is partially metabolized.
Side Effects
Contraindications
- Patients with known hypersensitivity to Imipenem, Cilastatin, or any component of the formulation.
- Patients with a history of severe hypersensitivity reactions to other beta-lactam antibiotics (e.g., penicillins, cephalosporins).
Drug Interactions
Probenecid
Increases plasma levels and prolongs the half-life of both Imipenem and Cilastatin.
Ganciclovir
Concomitant use with Imipenem/Cilastatin has been associated with generalized seizures.
Cyclosporine
Possible increased cyclosporine levels with concomitant use.
Valproic acid
Carbapenems, including Imipenem/Cilastatin, may decrease valproic acid plasma concentrations, leading to loss of seizure control.
Storage
Store dry powder vials below 25°C (77°F) in original packaging, protected from light and moisture. Do not freeze. Reconstituted solutions should be used immediately or refrigerated and used within specific timeframes.
Overdose
In case of overdose, discontinue the drug and provide supportive care. Imipenem/Cilastatin can be removed by hemodialysis.
Pregnancy & Lactation
Pregnancy Category C. Use only if the potential benefit justifies the potential risk to the fetus. Excreted in breast milk; use with caution in nursing mothers, considering the potential risks to the infant.
Frequently Asked Questions
Common questions about this medicine
Pack Sizes
Shelf Life
Typically 24-36 months from manufacturing date for dry powder. Reconstituted solution shelf life is limited (e.g., 4 hours at room temperature, 24 hours refrigerated).
Availability
Available in hospitals and pharmacies
Approval Status
Approved by regulatory authorities (e.g., FDA, DGDA)
Patent Status
Generic available, original patent expired
WHO Essential Medicine
YesClinical Trials
Extensive clinical trials have established the efficacy and safety of Imipenem/Cilastatin across various severe bacterial infections.
Lab Monitoring
- Renal function tests (creatinine, BUN) for patients with renal impairment or prolonged therapy.
- Liver function tests (ALT, AST) periodically.
- Complete blood count (CBC) with prolonged therapy.
Doctor Notes
- Administer slowly by IV infusion to minimize local irritation and systemic side effects.
- Careful dosage adjustment is crucial in patients with renal impairment to prevent accumulation and reduce the risk of CNS toxicity (e.g., seizures).
- Monitor patients for hypersensitivity reactions (including cross-reactivity with other beta-lactams) and signs of superinfection.
Patient Guidelines
- Complete the full course of antibiotic treatment as prescribed, even if symptoms improve.
- Report any severe diarrhea, skin rash, or signs of an allergic reaction immediately.
- Inform your doctor about all other medications you are taking, including over-the-counter drugs and herbal supplements.
Missed Dose Advice
If a dose is missed, administer it as soon as possible. However, if it is almost time for the next scheduled dose, skip the missed dose and resume your regular dosing schedule. Do not double the dose.
Driving Precautions
May cause dizziness or seizures. Patients should be advised to exercise caution when driving or operating machinery until they know how the medication affects them.
Lifestyle Advice
- Maintain adequate hydration during treatment.
- Avoid alcohol if it causes gastrointestinal upset or exacerbates side effects.
Alternative Medicines in Bangladesh
Similar medicines available in the market
Global Brand Names
International brand names for this medicine
Related
Medicines
Explore similar medicines to find the best option for your healthcare needs.
Avloquin-H
General Pharmaceuticals Ltd.
Lotenate Plus
General Pharmaceuticals Ltd.
Axovit
Reputable Pharma Ltd.
Azelec
Square Pharmaceuticals Ltd.
Azi S
Square Pharmaceuticals Ltd.
Exalin
Square Pharmaceuticals Ltd.
Azilpres
Specific manufacturer varies by region (e.g., Square Pharmaceuticals Ltd. in BD for a generic Azilsartan product)
Exipain
Acme Laboratories Ltd.
Timozin
MediCorp Pharma Ltd.
Exopan
Square Pharmaceuticals Ltd.