Does IMIPENEM Cause Incorrect product administration duration? 10 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 10 reports of Incorrect product administration duration have been filed in association with IMIPENEM. This represents 0.5% of all adverse event reports for IMIPENEM.
10
Reports of Incorrect product administration duration with IMIPENEM
0.5%
of all IMIPENEM reports
6
Deaths
4
Hospitalizations
How Dangerous Is Incorrect product administration duration From IMIPENEM?
Of the 10 reports, 6 (60.0%) resulted in death, 4 (40.0%) required hospitalization.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for IMIPENEM. However, 10 reports have been filed with the FAERS database.
What Other Side Effects Does IMIPENEM Cause?
Drug ineffective (351)
Off label use (202)
Condition aggravated (138)
Vomiting (137)
Drug resistance (117)
Nausea (111)
Dyspnoea (97)
Diarrhoea (90)
Pyrexia (90)
Product use in unapproved indication (85)
What Other Drugs Cause Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which IMIPENEM Alternatives Have Lower Incorrect product administration duration Risk?
IMIPENEM vs IMIPRAMINE
IMIPENEM vs IMIQUIMOD
IMIPENEM vs IMITREX
IMIPENEM vs IMMUNE GLOBULIN NOS
IMIPENEM vs IMPLANON