Does CABOTEGRAVIR\RILPIVIRINE Cause Product storage error? 168 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 168 reports of Product storage error have been filed in association with CABOTEGRAVIR\RILPIVIRINE. This represents 3.3% of all adverse event reports for CABOTEGRAVIR\RILPIVIRINE.
168
Reports of Product storage error with CABOTEGRAVIR\RILPIVIRINE
3.3%
of all CABOTEGRAVIR\RILPIVIRINE reports
0
Deaths
2
Hospitalizations
How Dangerous Is Product storage error From CABOTEGRAVIR\RILPIVIRINE?
Of the 168 reports, 2 (1.2%) 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\RILPIVIRINE. However, 168 reports have been filed with the FAERS database.
What Other Side Effects Does CABOTEGRAVIR\RILPIVIRINE Cause?
Product dose omission issue (655)
Injection site pain (545)
Viral load increased (428)
Off label use (366)
Pain (256)
Virologic failure (255)
Product use in unapproved therapeutic environment (239)
Pathogen resistance (202)
Inappropriate schedule of product administration (162)
Product complaint (158)
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\RILPIVIRINE Alternatives Have Lower Product storage error Risk?
CABOTEGRAVIR\RILPIVIRINE vs CABOZANTINIB
CABOTEGRAVIR\RILPIVIRINE vs CABOZANTINIB S-MALATE
CABOTEGRAVIR\RILPIVIRINE vs CAFFEINE
CABOTEGRAVIR\RILPIVIRINE vs CALASPARGASE PEGOL
CABOTEGRAVIR\RILPIVIRINE vs CALASPARGASE PEGOL-MKNL