Does IPRATROPIUM\IPRATROPIUM ANHYDROUS Cause Product dose omission issue? 69 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 69 reports of Product dose omission issue have been filed in association with IPRATROPIUM\IPRATROPIUM ANHYDROUS. This represents 16.3% of all adverse event reports for IPRATROPIUM\IPRATROPIUM ANHYDROUS.
69
Reports of Product dose omission issue with IPRATROPIUM\IPRATROPIUM ANHYDROUS
16.3%
of all IPRATROPIUM\IPRATROPIUM ANHYDROUS reports
3
Deaths
4
Hospitalizations
How Dangerous Is Product dose omission issue From IPRATROPIUM\IPRATROPIUM ANHYDROUS?
Of the 69 reports, 3 (4.3%) resulted in death, 4 (5.8%) required hospitalization, and 3 (4.3%) 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\IPRATROPIUM ANHYDROUS. However, 69 reports have been filed with the FAERS database.
What Other Side Effects Does IPRATROPIUM\IPRATROPIUM ANHYDROUS Cause?
Product delivery mechanism issue (105)
Dyspnoea (77)
Off label use (69)
Condition aggravated (62)
Vomiting (61)
Abdominal distension (59)
Nausea (56)
Drug ineffective (54)
No adverse event (54)
Dry mouth (52)
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\IPRATROPIUM ANHYDROUS Alternatives Have Lower Product dose omission issue Risk?
IPRATROPIUM\IPRATROPIUM ANHYDROUS vs IPTACOPAN
IPRATROPIUM\IPRATROPIUM ANHYDROUS vs IRBESARTAN
IPRATROPIUM\IPRATROPIUM ANHYDROUS vs IRINOTECAN
IPRATROPIUM\IPRATROPIUM ANHYDROUS vs IRON
IPRATROPIUM\IPRATROPIUM ANHYDROUS vs IRON DEXTRAN