Note: This document contains side effect information about cephalexin. Some dosage forms listed on this page may not apply to the brand name Keflex.
Applies to cephalexin: oral capsules, oral for suspension.
Side effects include:
Adverse GI effects, including diarrhea, nausea, vomiting, dyspepsia, gastritis, abdominal pain.
For Healthcare Professionals
Applies to cephalexin: oral capsule, oral powder for reconstitution, oral tablet, oral tablet dispersible.
General
The most commonly reported side effects included diarrhea, dyspepsia, gastritis, nausea, and vomiting.[Ref]
Gastrointestinal
Frequency not reported: Diarrhea, nausea, vomiting, dyspepsia, gastritis, abdominal pain, anal pruritus, Clostridium difficile-associated diarrhea/colitis/pseudomembranous colitis
Postmarketing reports: Colitis[Ref]
Hematologic
Frequency not reported: Direct Coombs' test seroconversion, decreased prothrombin activity/prolonged prothrombin time, eosinophilia, neutropenia, thrombocytopenia, hemolytic anemia
Postmarketing reports: Aplastic anemia, pancytopenia, leukopenia, agranulocytosis[Ref]
Dermatologic
Frequency not reported: Urticaria, rash, erythema multiforme, Stevens Johnson syndrome, toxic epidermal necrolysis/exanthematic necrolysis[Ref]
Hepatic
Frequency not reported: Transient hepatitis, cholestatic jaundice, AST and ALT elevations
Postmarketing reports: Increased bilirubin[Ref]
Hypersensitivity
Frequency not reported: Hypersensitivity/allergic reactions, angioedema, anaphylaxis[Ref]
Allergic reactions (including urticaria and angioedema) usually subsided upon treatment discontinuation.[Ref]
Genitourinary
Frequency not reported: Genital pruritus, genital candidiasis, vulvovaginitis/vaginitis and vaginal discharge[Ref]
Nervous system
Frequency not reported: Seizure, dizziness, headache[Ref]
Psychiatric
Frequency not reported: Agitation, confusion, hallucinations[Ref]
Musculoskeletal
Frequency not reported: Arthralgia, arthritis, joint disorder[Ref]
Renal
Frequency not reported: Reversible interstitial nephritis
Postmarketing reports: Renal dysfunction, toxic nephropathy, increased blood urea nitrogen, increased creatinine[Ref]
Other
Frequency not reported: Fatigue
Postmarketing reports: Fever[Ref]
Immunologic
Frequency not reported: Development of drug-resistant bacteria development[Ref]
Metabolic
Postmarketing reports: Increased alkaline phosphatase, increased lactate dehydrogenase (LDH)[Ref]
Cardiovascular
Postmarketing reports: Hemorrhage[Ref]