"The Centers for Disease Control and Prevention (CDC) is closely following new reports of the mosquito-borne chikungunya (chik-un-GUHN-ya) virus among residents of the French side of St. Martin in the Caribbean. While outbreaks of chikungunya "...
The following reactions have been reported:
Gastrointestinal: Diarrhea, oral candidiasis (oral thrush), vomiting, nausea, stomach cramps, anorexia and pseudomembranous colitis. Onset of pseudomembranous colitis symptoms may occur during or after antibiotic treatment (see WARNINGS). Nausea and vomiting have been reported rarely.
Hepatic: Transient rise in SGOT, SGPT, and alkaline phosphatase levels has been observed. As with other cephalosporins, reports of hepatitis have been received.
Renal: As with other cephalosporins, reports of increased BUN and creatinine levels, as well as renal failure, have been received.
Local Reactions: Rare instances of phlebitis have been reported at site of injection. Some induration has occurred.
Other Reactions:Genital and anal pruritus (including vulvar pruritus, genital moniliasis, and vaginitis).
Read the Cefazolin Injection (cefazolin and dextrose for injection) Side Effects Center for a complete guide to possible side effects
Probenecid may decrease renal tubular secretion of cephalosporins when used concurrently, resulting in increased and more prolonged cephalosporin blood levels.
Drug/Laboratory Test Interactions
A false positive reaction for glucose in the urine may occur with Benedict's solution, Fehling's solution or with Clinitest® tablets, but not with enzyme-based tests such as Clinistix®.
Positive direct and indirect antiglobulin (Coombs) tests have occurred; these may also occur in neonates whose mothers received cephalosporins before delivery.
Last reviewed on RxList: 2/9/2009
This monograph has been modified to include the generic and brand name in many instances.
Additional Cefazolin Injection Information
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You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.
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