Does NINTEDANIB Cause Wrong technique in product usage process? 27 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 27 reports of Wrong technique in product usage process have been filed in association with NINTEDANIB. This represents 0.1% of all adverse event reports for NINTEDANIB.
27
Reports of Wrong technique in product usage process with NINTEDANIB
0.1%
of all NINTEDANIB reports
1
Deaths
8
Hospitalizations
How Dangerous Is Wrong technique in product usage process From NINTEDANIB?
Of the 27 reports, 1 (3.7%) resulted in death, 8 (29.6%) required hospitalization, and 1 (3.7%) were considered life-threatening.
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 NINTEDANIB. However, 27 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 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 NINTEDANIB Alternatives Have Lower Wrong technique in product usage process Risk?
NINTEDANIB vs NINTEDANIB ESYLATE
NINTEDANIB vs NIRAPARIB
NINTEDANIB vs NIRMATRELVIR\RITONAVIR
NINTEDANIB vs NIROGACESTAT
NINTEDANIB vs NIROGACESTAT HYDROBROMIDE