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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does VANDETANIB Cause Drug dose omission? 6 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Drug dose omission have been filed in association with VANDETANIB (CAPRELSA). This represents 0.5% of all adverse event reports for VANDETANIB.

6
Reports of Drug dose omission with VANDETANIB
0.5%
of all VANDETANIB reports
0
Deaths
1
Hospitalizations

How Dangerous Is Drug dose omission From VANDETANIB?

Of the 6 reports, 1 (16.7%) required hospitalization.

Is Drug dose omission Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for VANDETANIB. However, 6 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 Drug dose omission?

ETANERCEPT (10,871) CINACALCET (8,683) EVOLOCUMAB (4,914) ADALIMUMAB (3,993) INSULIN LISPRO (3,063) GOLIMUMAB (2,652) TERIPARATIDE (2,616) APREMILAST (2,466) ALBUTEROL (2,309) FLUTICASONE\SALMETEROL (2,153)

Which VANDETANIB Alternatives Have Lower Drug 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

Related Pages

VANDETANIB Full Profile All Drug dose omission Reports All Drugs Causing Drug dose omission VANDETANIB Demographics