Does ERTAPENEM Cause Incorrect product administration duration? 17 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 17 reports of Incorrect product administration duration have been filed in association with ERTAPENEM (INVANZ). This represents 0.4% of all adverse event reports for ERTAPENEM.
17
Reports of Incorrect product administration duration with ERTAPENEM
0.4%
of all ERTAPENEM reports
0
Deaths
1
Hospitalizations
How Dangerous Is Incorrect product administration duration From ERTAPENEM?
Of the 17 reports, 1 (5.9%) required hospitalization, and 1 (5.9%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ERTAPENEM. However, 17 reports have been filed with the FAERS database.
What Other Side Effects Does ERTAPENEM Cause?
Drug ineffective (1,001)
Macular degeneration (776)
Off label use (372)
Product use in unapproved indication (346)
Pyrexia (279)
Nausea (277)
Confusional state (263)
Pain (255)
Malaise (220)
Weight decreased (220)
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 ERTAPENEM Alternatives Have Lower Incorrect product administration duration Risk?
ERTAPENEM vs ERTUGLIFLOZIN PIDOLATE
ERTAPENEM vs ERYTHROMYCIN
ERTAPENEM vs ERYTHROMYCIN ETHYLSUCCINATE
ERTAPENEM vs ERYTHROMYCIN LACTOBIONATE
ERTAPENEM vs ERYTHROPOIETIN