Does IPRATROPIUM Cause Product dose omission? 48 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 48 reports of Product dose omission have been filed in association with IPRATROPIUM (Ipratropium bromide). This represents 0.6% of all adverse event reports for IPRATROPIUM.
48
Reports of Product dose omission with IPRATROPIUM
0.6%
of all IPRATROPIUM reports
0
Deaths
4
Hospitalizations
How Dangerous Is Product dose omission From IPRATROPIUM?
Of the 48 reports, 4 (8.3%) required hospitalization.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for IPRATROPIUM. However, 48 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?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which IPRATROPIUM Alternatives Have Lower Product dose omission Risk?
IPRATROPIUM vs IPRATROPIUM\IPRATROPIUM ANHYDROUS
IPRATROPIUM vs IPTACOPAN
IPRATROPIUM vs IRBESARTAN
IPRATROPIUM vs IRINOTECAN
IPRATROPIUM vs IRON