Does CABOTEGRAVIR Cause Product preparation issue? 29 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 29 reports of Product preparation issue have been filed in association with CABOTEGRAVIR (Apretude). This represents 0.4% of all adverse event reports for CABOTEGRAVIR.
29
Reports of Product preparation issue with CABOTEGRAVIR
0.4%
of all CABOTEGRAVIR reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product preparation issue From CABOTEGRAVIR?
Of the 29 reports.
Is Product preparation issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CABOTEGRAVIR. However, 29 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 preparation issue?
ONABOTULINUMTOXINA (677)
COAGULATION FACTOR IX HUMAN\COAGULATION FACTOR VII HUMAN\COAGULATION FACTOR X HUMAN\PROTEIN C\PROTEIN S HUMAN\PROTHROMBIN (252)
HUMAN C1-ESTERASE INHIBITOR (238)
SOMATROPIN (200)
INCOBOTULINUMTOXINA (174)
STIRIPENTOL (129)
TESAMORELIN (119)
ABATACEPT (115)
INFLIXIMAB (101)
ABOBOTULINUMTOXINA (91)
Which CABOTEGRAVIR Alternatives Have Lower Product preparation issue Risk?
CABOTEGRAVIR vs CABOTEGRAVIR\RILPIVIRINE
CABOTEGRAVIR vs CABOZANTINIB
CABOTEGRAVIR vs CABOZANTINIB S-MALATE
CABOTEGRAVIR vs CAFFEINE
CABOTEGRAVIR vs CALASPARGASE PEGOL