Does GLYCOPYRROLATE Cause Device power source issue? 39 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 39 reports of Device power source issue have been filed in association with GLYCOPYRROLATE (GLYCOPYRROLATE). This represents 0.8% of all adverse event reports for GLYCOPYRROLATE.
39
Reports of Device power source issue with GLYCOPYRROLATE
0.8%
of all GLYCOPYRROLATE reports
1
Deaths
2
Hospitalizations
How Dangerous Is Device power source issue From GLYCOPYRROLATE?
Of the 39 reports, 1 (2.6%) resulted in death, 2 (5.1%) required hospitalization.
Is Device power source issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GLYCOPYRROLATE. However, 39 reports have been filed with the FAERS database.
What Other Side Effects Does GLYCOPYRROLATE Cause?
Dyspnoea (1,499)
Asthma (1,033)
Cough (950)
Wheezing (782)
Pneumonia (454)
Malaise (452)
Drug ineffective (448)
Chronic obstructive pulmonary disease (407)
Productive cough (384)
Chest discomfort (362)
What Other Drugs Cause Device power source issue?
SOMATROPIN (1,219)
PEGFILGRASTIM (486)
TREPROSTINIL (299)
CARBIDOPA\LEVODOPA (62)
ETANERCEPT (54)
BACLOFEN (50)
DEVICE (20)
FOSCARBIDOPA\FOSLEVODOPA (14)
INTERFERON BETA-1B (13)
LECITHIN\POLOXAMER 407 (11)
Which GLYCOPYRROLATE Alternatives Have Lower Device power source issue Risk?
GLYCOPYRROLATE vs GLYCOPYRROLATE\INDACATEROL
GLYCOPYRROLATE vs GLYCOPYRROLATE\INDACATEROL\MOMETASONE FUROATE
GLYCOPYRROLATE vs GLYCOPYRRONIUM
GLYCOPYRROLATE vs GLYCOPYRRONIUM\INDACATEROL
GLYCOPYRROLATE vs GOLD