Does VANDETANIB Cause Intentional dose omission? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Intentional dose omission have been filed in association with VANDETANIB (CAPRELSA). This represents 0.6% of all adverse event reports for VANDETANIB.
7
Reports of Intentional dose omission with VANDETANIB
0.6%
of all VANDETANIB reports
0
Deaths
1
Hospitalizations
How Dangerous Is Intentional dose omission From VANDETANIB?
Of the 7 reports, 1 (14.3%) required hospitalization.
Is Intentional dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for VANDETANIB. However, 7 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 Intentional dose omission?
DUPILUMAB (2,269)
CERTOLIZUMAB PEGOL (1,253)
ADALIMUMAB (845)
TOFACITINIB (845)
INFLIXIMAB (815)
ABALOPARATIDE (623)
ETANERCEPT (615)
AMBRISENTAN (595)
SODIUM OXYBATE (580)
CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (518)
Which VANDETANIB Alternatives Have Lower Intentional dose omission Risk?
VANDETANIB vs VARDENAFIL
VANDETANIB vs VARENICLINE
VANDETANIB vs VARICELLA-ZOSTER VIRUS STRAIN OKA/MERCK LIVE ANTIGEN
VANDETANIB vs VASOPRESSIN
VANDETANIB vs VECTIBIX