Does PROAIR HFA Cause Dyspnoea? 64 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 64 reports of Dyspnoea have been filed in association with PROAIR HFA. This represents 19.6% of all adverse event reports for PROAIR HFA.
64
Reports of Dyspnoea with PROAIR HFA
19.6%
of all PROAIR HFA reports
1
Deaths
10
Hospitalizations
How Dangerous Is Dyspnoea From PROAIR HFA?
Of the 64 reports, 1 (1.6%) resulted in death, 10 (15.6%) required hospitalization.
Is Dyspnoea Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PROAIR HFA. However, 64 reports have been filed with the FAERS database.
What Other Side Effects Does PROAIR HFA Cause?
Drug ineffective (105)
Cough (43)
Device malfunction (38)
Asthma (29)
Wheezing (19)
Product quality issue (16)
Dizziness (15)
Drug effect decreased (15)
Malaise (14)
Chest discomfort (13)
What Other Drugs Cause Dyspnoea?
ALBUTEROL (21,856)
TREPROSTINIL (16,348)
AMBRISENTAN (13,367)
PREDNISONE (12,830)
BUDESONIDE\FORMOTEROL (11,158)
TIOTROPIUM (10,863)
ADALIMUMAB (10,547)
DUPILUMAB (10,310)
FLUTICASONE\SALMETEROL (9,783)
MEPOLIZUMAB (9,192)
Which PROAIR HFA Alternatives Have Lower Dyspnoea Risk?
PROAIR HFA vs PROBIOTICS NOS
PROAIR HFA vs PROBUCOL
PROAIR HFA vs PROCAINAMIDE
PROAIR HFA vs PROCAINE
PROAIR HFA vs PROCARBAZINE