Does IPRATROPIUM Cause Product dose omission issue? 320 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 320 reports of Product dose omission issue have been filed in association with IPRATROPIUM (Ipratropium bromide). This represents 4.2% of all adverse event reports for IPRATROPIUM.
320
Reports of Product dose omission issue with IPRATROPIUM
4.2%
of all IPRATROPIUM reports
55
Deaths
169
Hospitalizations
How Dangerous Is Product dose omission issue From IPRATROPIUM?
Of the 320 reports, 55 (17.2%) resulted in death, 169 (52.8%) required hospitalization, and 33 (10.3%) were considered life-threatening.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for IPRATROPIUM. However, 320 reports have been filed with the FAERS database.
What Other Side Effects Does IPRATROPIUM Cause?
Asthma (2,596)
Dyspnoea (2,450)
Wheezing (1,910)
Cough (1,315)
Therapeutic product effect incomplete (1,229)
Obstructive airways disorder (1,171)
Drug ineffective (1,057)
Pneumonia (931)
Loss of personal independence in daily activities (861)
Chest discomfort (785)
What Other Drugs Cause Product dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which IPRATROPIUM Alternatives Have Lower Product dose omission issue Risk?
IPRATROPIUM vs IPRATROPIUM\IPRATROPIUM ANHYDROUS
IPRATROPIUM vs IPTACOPAN
IPRATROPIUM vs IRBESARTAN
IPRATROPIUM vs IRINOTECAN
IPRATROPIUM vs IRON