Anthropometric Measurements as Predictors of Low Birth Weight Among Tanzanian Neonates: A Hospital-Based Study
November 7, 2025
Brand Name :
Merrem IV
Synonyms :
meropenem
Class :
Dosage Forms & StrengthsÂ
Powder for injectable solutionÂ
500mg/vialÂ
1g/vialÂ
Â
Indicated for Skin Structure / Complicated Skin Infections:
500mg intravenous thrice a day
Do not exceed 2g intravenous thrice a day
1g intravenous thrice a day
Do not exceed 2g intravenous thrice a day
(Off Label):
Fluoroquinolone and 500 mg intravenously every 8 hours for around five days
Dosage Forms & StrengthsÂ
Powder for injectable solutionÂ
500mg/vialÂ
1g/vialÂ
≥3 months: 20 mg/kg intravenous thrice a day; Do not exceed 1 g every 8 hours
<3 months:
Infants <32 weeks GA and PNA <2 weeks: 20mg/kg intravenous twice a day
Infants <32 weeks GA and PNA ≥2 weeks: 20 mg/kg intravenous thrice a day
Infants ≥32 weeks GA and PNA <2 weeks: 20 mg/kg intravenous thrice a day
Infants ≥32 weeks GA and PNA ≥2 weeks: 30 mg/kg intravenous thrice a day
Infuse intravenously for 30 minutes
Indicated for Skin Structure / Complicated Skin Infections:
≥3 months: 10 mg/kg intravenous thrice a day; Do not exceed 500 mg intravenous every 8 hours
Indicated for Bacterial Meningitis:
≥3 months: 40 mg/kg intravenous thrice a day; Do not exceed 2 g every 8 hours
Refer adult dosingÂ
may decrease the therapeutic effect of Antibiotics
may decrease the therapeutic effect of antibiotics
may enhance the serum concentration of OAT1/3 Substrates
sodium picosulfate, citric acid, and magnesium oxideÂ
may decrease the therapeutic effect of Antibiotics
may enhance the serum concentration of OAT1/3 Substrates
may enhance the serum concentration of meropenem
may enhance the serum concentration of OAT1/3 Substrates
may enhance the serum concentration of OAT1/3 Substrates
may enhance the serum concentration of OAT1/3 Substrates
may decrease the therapeutic effect of antibiotics
may decrease the therapeutic effect of antibiotics
may decrease the therapeutic effect of antibiotics
may decrease the therapeutic effect of antibiotics
may decrease the therapeutic effect of antibiotics
amoxicillin and clavulanate potassium
may decrease the therapeutic effect of antibiotics
bismuth subcitrate, metronidazole and tetracycline
may decrease the therapeutic effect of antibiotics
may decrease the therapeutic effect of antibiotics
may decrease the therapeutic effect of antibiotics
It may enhance the risk of adverse effects when combined with Diagnostic agents
It may enhance the risk of adverse effects when combined with Diagnostic agents
It may enhance the risk of adverse effects when combined with Diagnostic agents
It may enhance the risk of adverse effects when combined with Diagnostic agents
It may enhance the risk of adverse effects when combined with Diagnostic agents
Actions and Spectrum:Â
Frequency definedÂ
1-10%Â
Diarrhea (4-5%)Â
Rash (2-3%)Â Â
Inflammation at the injection site (2%)Â
Oral moniliasis (≤2% in pediatric patients)Â
Apnea (1%)Â
Glossitis (1%)Â
Injection-site reaction (1%)Â
Pruritus (1%)Â
Constipation (1-7%)Â
Nausea or vomiting (1-4%)Â
Headache (2%)Â
Sepsis (2%)Â
Bleeding (1.2%)Â
Constipation (1%)Â
Phlebitis or thrombophlebitis (1%)Â
Septic shock (1%)Â Â
<1%Â
AngioedemaÂ
Hypersensitivity reactionÂ
LeukopeniaÂ
Pleural effusionÂ
Toxic epidermal necrolysisÂ
AgranulocytosisÂ
Erythema multiformeÂ
HypokalemiaÂ
NeutropeniaÂ
Stevens-Johnson syndrome Â
Post-marketing reportsÂ
Toxic epidermal necrolysisÂ
Stevens-Johnson syndromeÂ
Erythema multiforme and acute generalized exanthematous pustulosisÂ
Drug reaction with eosinophilia and systemic symptoms (DRESS)Â
Contraindications/caution:Â
Contraindications:Â
meropenem is generally considered safe and well-tolerated, but some situations may be contraindicated or should be used cautiously. meropenem is contraindicated in patients with known hypersensitivity to carbapenems or beta-lactam antibiotics. It should also be used cautiously in patients with a history of allergic reactions to other beta-lactam antibiotics, such as penicillins or cephalosporins.Â
Caution:Â
Pregnancy consideration: Insufficient data available.Â
meropenem is also not recommended during pregnancy unless the potential benefits outweigh the potential risksÂ
Lactation: Excretion of the drug in human breast milk is unknown, so caution should be exercised when administering the drug to nursing mothers.Â
Pregnancy category:Â
Category A: well-controlled and Satisfactory studies show no risk to the fetus in the first or later trimester.  Â
Category B: there was no evidence of risk to the fetus in animal studies, and there were not enough studies on pregnant women.Â
Category C: there was evidence of risk of adverse effects in animal reproduction studies, and no adequate evidence in human studies must take care of potential risks in pregnant women.   Â
Category D: adequate data available with sufficient evidence of human fetal risk from various platforms, but despite the potential risk, and used only in emergency cases for potential benefits.   Â
Category X: Drugs listed in this category outweigh the risks over benefits. Hence these categories of drugs need to be avoided by pregnant women.   Â
Category N: There is no data available for the drug under this categoryÂ
Pharmacology:Â
meropenem is a beta-lactam antibiotic that belongs to the carbapenem class of antibiotics. It works by inhibiting bacterial cell wall synthesis, ultimately leading to cell death. Â
meropenem is a bactericidal antibiotic that is effective against a broad spectrum of gram-positive and gram-negative bacteria. It is more stable to degradation by bacterial enzymes than other carbapenems, allowing for greater efficacy against some resistant bacteria.Â
Pharmacodynamics:Â
Pharmacokinetics:Â
AbsorptionÂ
meropenem is administered intravenously, and it is well-absorbed after intravenous infusion. Â
DistributionÂ
meropenem has a large volume of distribution, which is approximately 15-20 L in adults and 0.3-0.4 L/kg in children. It penetrates well into most body fluids and tissues, including the cerebrospinal fluid, whose concentrations approximate those in plasma. The drug is minimally protein bound, with approximately 2% bound to plasma proteins. Â
MetabolismÂ
meropenem is metabolized in the liver to an inactive open beta-lactam form, excreted in the urine. Â
Elimination and ExcretionÂ
 The drug has a relatively short half-life of approximately 1-1.5 hours in patients with normal renal function. Its elimination depends on renal function, and approximately 25% of meropenem is excreted unchanged in the urine, with the remainder excreted as inactive metabolites. The drug is cleared primarily by glomerular filtration, and dose adjustments are necessary for patients with renal impairment.Â
Administration:Â
Patient information leafletÂ
Generic Name: meropenemÂ
Why do we use meropenem?Â
meropenem is a broad-spectrum antibiotic that is used to treat a wide range of bacterial infections, including:Â