Does ABACAVIR\LAMIVUDINE Cause Product quality issue? 9 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Product quality issue have been filed in association with ABACAVIR\LAMIVUDINE. This represents 0.2% of all adverse event reports for ABACAVIR\LAMIVUDINE.
9
Reports of Product quality issue with ABACAVIR\LAMIVUDINE
0.2%
of all ABACAVIR\LAMIVUDINE reports
0
Deaths
3
Hospitalizations
How Dangerous Is Product quality issue From ABACAVIR\LAMIVUDINE?
Of the 9 reports, 3 (33.3%) required hospitalization.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ABACAVIR\LAMIVUDINE. However, 9 reports have been filed with the FAERS database.
What Other Side Effects Does ABACAVIR\LAMIVUDINE Cause?
Exposure during pregnancy (593)
Pyrexia (450)
Rash (390)
Foetal exposure during pregnancy (373)
Hypertension (325)
Headache (316)
Hypersensitivity (289)
Pain (271)
Thrombocytopenia (271)
Off label use (267)
What Other Drugs Cause Product quality issue?
ETONOGESTREL (4,651)
ALBUTEROL (4,466)
TIOTROPIUM (3,821)
MOMETASONE FUROATE (3,406)
LIDOCAINE (3,126)
FLUTICASONE\SALMETEROL (2,986)
FORMOTEROL\MOMETASONE FUROATE (2,458)
FENTANYL (2,450)
NICOTINE (1,987)
EXENATIDE (1,839)
Which ABACAVIR\LAMIVUDINE Alternatives Have Lower Product quality issue Risk?
ABACAVIR\LAMIVUDINE vs ABACAVIR\LAMIVUDINE\ZIDOVUDINE
ABACAVIR\LAMIVUDINE vs ABALOPARATIDE
ABACAVIR\LAMIVUDINE vs ABATACEPT
ABACAVIR\LAMIVUDINE vs ABATACEPT SUBQ /ML
ABACAVIR\LAMIVUDINE vs ABCIXIMAB