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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 Wrong technique in product usage process? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Wrong technique in product usage process have been filed in association with VANDETANIB (CAPRELSA). This represents 0.4% of all adverse event reports for VANDETANIB.

5
Reports of Wrong technique in product usage process with VANDETANIB
0.4%
of all VANDETANIB reports
0
Deaths
1
Hospitalizations

How Dangerous Is Wrong technique in product usage process From VANDETANIB?

Of the 5 reports, 1 (20.0%) required hospitalization.

Is Wrong technique in product usage process Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for VANDETANIB. However, 5 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 Wrong technique in product usage process?

EVOLOCUMAB (21,664) ALBUTEROL (17,114) ADALIMUMAB (11,766) PEGFILGRASTIM (10,217) ETANERCEPT (9,835) ERENUMAB-AOOE (9,359) SACUBITRIL\VALSARTAN (8,022) LEUPROLIDE (5,062) FENTANYL (2,812) SEMAGLUTIDE (2,538)

Which VANDETANIB Alternatives Have Lower Wrong technique in product usage process 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 Wrong technique in product usage process Reports All Drugs Causing Wrong technique in product usage process VANDETANIB Demographics