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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 NINTEDANIB Cause Product quality issue? 26 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 26 reports of Product quality issue have been filed in association with NINTEDANIB. This represents 0.1% of all adverse event reports for NINTEDANIB.

26
Reports of Product quality issue with NINTEDANIB
0.1%
of all NINTEDANIB reports
6
Deaths
11
Hospitalizations

How Dangerous Is Product quality issue From NINTEDANIB?

Of the 26 reports, 6 (23.1%) resulted in death, 11 (42.3%) required hospitalization.

Is Product quality issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for NINTEDANIB. However, 26 reports have been filed with the FAERS database.

What Other Side Effects Does NINTEDANIB Cause?

Diarrhoea (9,103) Nausea (4,198) Dyspnoea (3,080) Decreased appetite (2,832) Death (2,790) Weight decreased (2,628) Vomiting (2,524) Fatigue (2,511) Cough (2,193) Idiopathic pulmonary fibrosis (1,905)

What Other Drugs Cause Product quality issue?

ETONOGESTREL (4,651) ALBUTEROL (4,466) TIOTROPIUM (3,821) MOMETASONE FUROATE (3,406) LIDOCAINE (3,126) FLUTICASONE\SALMETEROL (2,986) FORMOTEROL\MOMETASONE FUROATE (2,458) FENTANYL (2,450) NICOTINE (1,987) EXENATIDE (1,839)

Which NINTEDANIB Alternatives Have Lower Product quality issue Risk?

NINTEDANIB vs NINTEDANIB ESYLATE NINTEDANIB vs NIRAPARIB NINTEDANIB vs NIRMATRELVIR\RITONAVIR NINTEDANIB vs NIROGACESTAT NINTEDANIB vs NIROGACESTAT HYDROBROMIDE

Related Pages

NINTEDANIB Full Profile All Product quality issue Reports All Drugs Causing Product quality issue NINTEDANIB Demographics