Does CABOTEGRAVIR Cause Product storage error? 180 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 180 reports of Product storage error have been filed in association with CABOTEGRAVIR (Apretude). This represents 2.2% of all adverse event reports for CABOTEGRAVIR.
180
Reports of Product storage error with CABOTEGRAVIR
2.2%
of all CABOTEGRAVIR reports
0
Deaths
2
Hospitalizations
How Dangerous Is Product storage error From CABOTEGRAVIR?
Of the 180 reports, 2 (1.1%) required hospitalization.
Is Product storage error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CABOTEGRAVIR. However, 180 reports have been filed with the FAERS database.
What Other Side Effects Does CABOTEGRAVIR Cause?
Product dose omission issue (1,121)
Off label use (1,049)
Injection site pain (924)
Viral load increased (452)
Pain (399)
Virologic failure (275)
Pathogen resistance (270)
Pyrexia (255)
Product use in unapproved therapeutic environment (234)
Inappropriate schedule of product administration (228)
What Other Drugs Cause Product storage error?
INSULIN GLARGINE (7,743)
EVOLOCUMAB (6,606)
ETANERCEPT (3,653)
DENOSUMAB (3,621)
ERENUMAB-AOOE (2,958)
DUPILUMAB (2,631)
ALBUTEROL (2,474)
ABATACEPT (2,101)
DARBEPOETIN ALFA (1,619)
INSULIN LISPRO (1,448)
Which CABOTEGRAVIR Alternatives Have Lower Product storage error Risk?
CABOTEGRAVIR vs CABOTEGRAVIR\RILPIVIRINE
CABOTEGRAVIR vs CABOZANTINIB
CABOTEGRAVIR vs CABOZANTINIB S-MALATE
CABOTEGRAVIR vs CAFFEINE
CABOTEGRAVIR vs CALASPARGASE PEGOL