Does TIOTROPIUM Cause Wrong technique in device usage process? 84 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 84 reports of Wrong technique in device usage process have been filed in association with TIOTROPIUM (Tiotropium Bromide). This represents 0.2% of all adverse event reports for TIOTROPIUM.
84
Reports of Wrong technique in device usage process with TIOTROPIUM
0.2%
of all TIOTROPIUM reports
0
Deaths
7
Hospitalizations
How Dangerous Is Wrong technique in device usage process From TIOTROPIUM?
Of the 84 reports, 7 (8.3%) required hospitalization.
Is Wrong technique in device usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TIOTROPIUM. However, 84 reports have been filed with the FAERS database.
What Other Side Effects Does TIOTROPIUM Cause?
Dyspnoea (10,863)
Incorrect route of drug administration (9,079)
Asthma (7,944)
Wheezing (5,361)
Therapeutic product effect incomplete (4,327)
Cough (4,202)
Product quality issue (3,821)
Drug ineffective (3,642)
Loss of personal independence in daily activities (3,414)
Pneumonia (3,046)
What Other Drugs Cause Wrong technique in device usage process?
ALBUTEROL (5,380)
SOMATROPIN (4,746)
EXENATIDE (3,255)
FLUTICASONE FUROATE\UMECLIDINIUM\VILANTEROL TRIFENATATE (2,673)
FLUTICASONE\SALMETEROL (2,259)
FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (2,197)
INSULIN GLARGINE (1,749)
UMECLIDINIUM\VILANTEROL TRIFENATATE (1,531)
BUDESONIDE\FORMOTEROL (1,481)
BELIMUMAB (1,347)
Which TIOTROPIUM Alternatives Have Lower Wrong technique in device usage process Risk?
TIOTROPIUM vs TIPIRACIL\TRIFLURIDINE
TIOTROPIUM vs TIPRANAVIR
TIOTROPIUM vs TIRAGOLUMAB
TIOTROPIUM vs TIRBANIBULIN
TIOTROPIUM vs TIROFIBAN