Does VANDETANIB Cause Product dose omission in error? 13 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 13 reports of Product dose omission in error have been filed in association with VANDETANIB (CAPRELSA). This represents 1.1% of all adverse event reports for VANDETANIB.
13
Reports of Product dose omission in error with VANDETANIB
1.1%
of all VANDETANIB reports
0
Deaths
1
Hospitalizations
How Dangerous Is Product dose omission in error From VANDETANIB?
Of the 13 reports, 1 (7.7%) required hospitalization.
Is Product dose omission in error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for VANDETANIB. However, 13 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 dose omission in error?
DUPILUMAB (7,586)
TOFACITINIB (2,461)
LENALIDOMIDE (618)
PALBOCICLIB (592)
DIROXIMEL (481)
ABALOPARATIDE (457)
NIRAPARIB (428)
RUXOLITINIB (425)
TERIFLUNOMIDE (371)
DIMETHYL (308)
Which VANDETANIB Alternatives Have Lower Product dose omission in error Risk?
VANDETANIB vs VARDENAFIL
VANDETANIB vs VARENICLINE
VANDETANIB vs VARICELLA-ZOSTER VIRUS STRAIN OKA/MERCK LIVE ANTIGEN
VANDETANIB vs VASOPRESSIN
VANDETANIB vs VECTIBIX