Does PROAIR HFA Cause Device malfunction? 38 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 38 reports of Device malfunction have been filed in association with PROAIR HFA. This represents 11.7% of all adverse event reports for PROAIR HFA.
38
Reports of Device malfunction with PROAIR HFA
11.7%
of all PROAIR HFA reports
0
Deaths
2
Hospitalizations
How Dangerous Is Device malfunction From PROAIR HFA?
Of the 38 reports, 2 (5.3%) required hospitalization.
Is Device malfunction Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PROAIR HFA. However, 38 reports have been filed with the FAERS database.
What Other Side Effects Does PROAIR HFA Cause?
Drug ineffective (105)
Dyspnoea (64)
Cough (43)
Asthma (29)
Wheezing (19)
Product quality issue (16)
Dizziness (15)
Drug effect decreased (15)
Malaise (14)
Chest discomfort (13)
What Other Drugs Cause Device malfunction?
PEGFILGRASTIM (6,818)
EXENATIDE (3,273)
BUDESONIDE\FORMOTEROL (2,771)
ABATACEPT (2,459)
SOMATROPIN (2,311)
GOLIMUMAB (2,293)
SECUKINUMAB (2,259)
ALBUTEROL (2,257)
GUSELKUMAB (1,410)
MOMETASONE FUROATE (1,332)
Which PROAIR HFA Alternatives Have Lower Device malfunction Risk?
PROAIR HFA vs PROBIOTICS NOS
PROAIR HFA vs PROBUCOL
PROAIR HFA vs PROCAINAMIDE
PROAIR HFA vs PROCAINE
PROAIR HFA vs PROCARBAZINE