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ADVERSE REACTIONS Following adverse reactions have been reported during treatment with meropenem:
common or very common Abdominal pain. diarrhea. headache. inflammation. nausea. skin reactions.
thrombocytosis. vomiting
Uncommon Agranulocytosis. antibiotic associated colitis. eosinophilia. hemolytic anemia. increased risk of
infection. leucopenia. neutropenia. paranesthesia. Severe cutaneous adverse reactions (SCARs) [ Severe cutaneous
adverse reaction (SCAR) is life-threatening. It consists of Stevens-Johnson syndrome/toxic epidermal necrolysis
(SJS/TEN), drug reaction with eosinophilia and systemic symptoms (DRESS), acute generalized exanthematous
pustulosis (AGEP), and generalized bullous fixed drug eruptions (GBFDE)].. thrombocytopenia. thrombophlebitis
Rare Seizure
CONTRAINDICATIONS Meropenem is contraindicated in patients:
1- With known hypersensitivity to meropenem or to any excipient of the product. –
2- Hypersensitive to any other carbapenem antibacterial agent.
3- Hypersensitivity reaction (e.g., acute anaphylactic shock) to any other type of β-lactams antibacterial
agent (e.g., Penicillin and Cephalosporins).
PRECAUTIONS:
1. PREGNANCY Use only if potential benefit outweighs risk—no information available.
2. BREAST FEEDING Unlikely to be absorbed (however, manufacturer advises avoid).
3. MONITORING REQUIREMENTS Manufacturer advises monitor liver function—risk of hepatotoxicity.
DRUG INTERACTIONS
Probenecid Co-administration of Meropenem I.V. with probenecid inhibits renal excretion of meropenem.
Valproic Acid Co-administration of Meropenem I.V. with valproic acid or divalproex sodium reduces the
serum concentration of valproic acid potentially increasing the risk of breakthrough seizures.
Oral Anti-coagulants (e.g., Warfarin)
Simultaneous administration of antibiotics with warfarin may augment its anti-coagulant effects. It is
recommended that the INR should be monitored frequently during and shortly after co-administration of
antibiotics with an oral anti-coagulant agent.
DOSAGE AND ADMINISTRATION
• Renal Dosing
•
• Dosage for adult patient with hepatic impairment:
o Adult No adjustment