Can Meropenem (generic name) cause thrombocytopenia in critically ill patients?

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Last updated: January 21, 2026View editorial policy

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Meropenem and Thrombocytopenia in Critically Ill Patients

Yes, meropenem can cause thrombocytopenia, particularly in patients with renal impairment, though no clinical bleeding has been reported in clinical trials. 1

FDA-Labeled Warning

The FDA label explicitly warns that thrombocytopenia has been observed in patients with renal impairment receiving meropenem, though importantly, no clinical bleeding was reported in these cases. 1 This is listed as a specific warning requiring monitoring in the official prescribing information. 1

Clinical Trial Evidence

Incidence and Characteristics

  • In clinical trials of 2,904 adult patients treated with meropenem, decreased platelets were reported as an adverse laboratory change occurring in greater than 0.2% of patients. 1

  • A comprehensive safety review of nearly 5,000 patients found that thrombocytosis (increased platelets) was actually more common (1.6%) than thrombocytopenia with meropenem use. 2

  • The most common meropenem-related adverse events were diarrhea (2.3%), rash (1.4%), and nausea/vomiting (1.4%), with thrombocytopenia being less frequently reported. 2

Risk Factors

The primary risk factor is renal impairment. 1 The FDA label specifically notes that patients with moderately severe renal impairment (creatinine clearance 10 to 26 mL/min) had increased incidence of multiple complications including thrombocytopenia. 1

Comparative Evidence in Critically Ill Patients

A 2013 randomized controlled trial in critically ill patients provides important context: 3

  • High exposure to broad-spectrum antimicrobials, including meropenem, did not result in increased thrombocytopenia compared to standard-of-care antimicrobial regimens. 3

  • In observational analyses from this trial, ciprofloxacin and piperacillin/tazobactam were associated with thrombocytopenia risk, but meropenem was not specifically implicated as a major contributor. 3

  • Thrombocytopenia (absolute or relative) was common in critically ill patients (35% developed absolute thrombocytopenia during ICU stay), but this was related to critical illness rather than specific antimicrobials. 3

Mechanism: Immune-Mediated Thrombocytopenia

A 2017 case report documented meropenem-induced immune thrombocytopenia (DITP) confirmed by laboratory testing: 4

  • The patient developed severe thrombocytopenia 8 days after meropenem administration. 4

  • Laboratory testing demonstrated that platelet antibodies were detected only in the presence of meropenem, with glycoprotein IIb/IIIa identified as the binding site. 4

  • This represents a drug-dependent antibody mechanism, similar to other drug-induced immune cytopenias. 4

Clinical Implications and Monitoring

When to Suspect Meropenem-Induced Thrombocytopenia

  • Acute thrombocytopenia developing during meropenem treatment, particularly 5-10 days after initiation. 4

  • Presence of renal impairment (creatinine clearance 10-26 mL/min or lower). 1

  • Exclusion of other common causes in critically ill patients: sepsis-related consumption, heparin-induced thrombocytopenia, disseminated intravascular coagulation. 5

Monitoring Recommendations

While not specific to meropenem, guidelines for critically ill patients recommend: 5

  • Monitor platelet count every 24-72 hours in the acute phase of critical illness. 5

  • This monitoring helps detect multiple potential causes of thrombocytopenia, including drug-induced cases. 5

Common Pitfalls

  • Do not assume all thrombocytopenia in critically ill patients is drug-related. Sepsis, DIC, and heparin-induced thrombocytopenia are more common causes. 5

  • Meropenem-induced thrombocytopenia is rare compared to its overall favorable safety profile in nearly 5,000 patients studied. 2

  • The absence of clinical bleeding in FDA-documented cases suggests the thrombocytopenia is typically mild to moderate. 1

  • Renal dose adjustment is critical to minimize risk, as accumulation in renal impairment increases adverse event risk. 1

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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