Does IPRATROPIUM\IPRATROPIUM ANHYDROUS Cause Device leakage? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Device leakage have been filed in association with IPRATROPIUM\IPRATROPIUM ANHYDROUS. This represents 1.9% of all adverse event reports for IPRATROPIUM\IPRATROPIUM ANHYDROUS.
8
Reports of Device leakage with IPRATROPIUM\IPRATROPIUM ANHYDROUS
1.9%
of all IPRATROPIUM\IPRATROPIUM ANHYDROUS reports
0
Deaths
0
Hospitalizations
How Dangerous Is Device leakage From IPRATROPIUM\IPRATROPIUM ANHYDROUS?
Of the 8 reports.
Is Device leakage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for IPRATROPIUM\IPRATROPIUM ANHYDROUS. However, 8 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)
Product dose omission issue (69)
Condition aggravated (62)
Vomiting (61)
Abdominal distension (59)
Nausea (56)
Drug ineffective (54)
No adverse event (54)
What Other Drugs Cause Device leakage?
SOMATROPIN (9,113)
LEUPROLIDE (5,861)
EXENATIDE (5,115)
PEGFILGRASTIM (1,380)
ALBIGLUTIDE (1,195)
SECUKINUMAB (910)
RISPERIDONE (878)
TREPROSTINIL (874)
DEVICE (795)
GUSELKUMAB (712)
Which IPRATROPIUM\IPRATROPIUM ANHYDROUS Alternatives Have Lower Device leakage 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