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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

LORACARBEF: 36 Adverse Event Reports & Safety Profile

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36
Total FAERS Reports
0
Deaths Reported
2
Hospitalizations
36
As Primary/Secondary Suspect
Apr 5, 1996
FDA Approved
Discontinued
Status

FDA Application: 050667 ·

First Report: 20031003 · Latest Report: 20031003

What Are the Most Common LORACARBEF Side Effects?

#1 Most Reported
Drug hypersensitivity
33 reports (91.7%)
#2 Most Reported
Rash
3 reports (8.3%)
#3 Most Reported
Tubulointerstitial nephritis
2 reports (5.6%)

All LORACARBEF Side Effects by Frequency

Side Effect Reports % of Total Deaths Hosp.
Drug hypersensitivity 33 91.7% 0 0

Who Reports LORACARBEF Side Effects? Age & Gender Data

Gender: 88.2% female, 11.8% male. Average age: 49.9 years. Most reports from: US. View detailed demographics →

Is LORACARBEF Getting Safer? Reports by Year

YearReportsDeathsHosp.
2003 1 0 0

View full timeline →

Official FDA Label for LORACARBEF

Official prescribing information from the FDA-approved drug label.