Does SALMETEROL Cause Device use error? 59 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 59 reports of Device use error have been filed in association with SALMETEROL (SEREVENT DISKUS). This represents 3.4% of all adverse event reports for SALMETEROL.
59
Reports of Device use error with SALMETEROL
3.4%
of all SALMETEROL reports
0
Deaths
3
Hospitalizations
How Dangerous Is Device use error From SALMETEROL?
Of the 59 reports, 3 (5.1%) required hospitalization.
Is Device use error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SALMETEROL. However, 59 reports have been filed with the FAERS database.
What Other Side Effects Does SALMETEROL Cause?
Dyspnoea (345)
Drug ineffective (315)
Asthma (274)
Cough (219)
Chest discomfort (188)
Wheezing (186)
Off label use (152)
Dysphonia (133)
Obstructive airways disorder (126)
Drug hypersensitivity (118)
What Other Drugs Cause Device use error?
PEGFILGRASTIM (6,001)
ALBUTEROL (5,215)
ALBIGLUTIDE (4,056)
EVOLOCUMAB (4,002)
SOMATROPIN (2,801)
FLUTICASONE\SALMETEROL (1,749)
FLUTICASONE (783)
FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (766)
ERENUMAB-AOOE (711)
ETANERCEPT (665)
Which SALMETEROL Alternatives Have Lower Device use error Risk?
SALMETEROL vs SAMSCA
SALMETEROL vs SANDOSTATIN LAR
SALMETEROL vs SANDOZ FENTANYL SYSTEM
SALMETEROL vs SAPROPTERIN
SALMETEROL vs SAQUINAVIR