Does VANDETANIB Cause Product use issue? 9 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Product use issue have been filed in association with VANDETANIB (CAPRELSA). This represents 0.8% of all adverse event reports for VANDETANIB.
9
Reports of Product use issue with VANDETANIB
0.8%
of all VANDETANIB reports
3
Deaths
1
Hospitalizations
How Dangerous Is Product use issue From VANDETANIB?
Of the 9 reports, 3 (33.3%) resulted in death, 1 (11.1%) required hospitalization, and 1 (11.1%) were considered life-threatening.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for VANDETANIB. However, 9 reports have been filed with the FAERS database.
What Other Side Effects Does VANDETANIB Cause?
Diarrhoea (216)
Fatigue (109)
Rash (101)
Electrocardiogram qt prolonged (89)
Hypertension (88)
Disease progression (62)
Acne (60)
Nausea (58)
Asthenia (52)
Headache (48)
What Other Drugs Cause Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
Which VANDETANIB Alternatives Have Lower Product use issue Risk?
VANDETANIB vs VARDENAFIL
VANDETANIB vs VARENICLINE
VANDETANIB vs VARICELLA-ZOSTER VIRUS STRAIN OKA/MERCK LIVE ANTIGEN
VANDETANIB vs VASOPRESSIN
VANDETANIB vs VECTIBIX