Does ALBUTEROL Cause Recalled product administered? 22 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 22 reports of Recalled product administered have been filed in association with ALBUTEROL (Albuterol Sulfate). This represents 0.0% of all adverse event reports for ALBUTEROL.
22
Reports of Recalled product administered with ALBUTEROL
0.0%
of all ALBUTEROL reports
2
Deaths
0
Hospitalizations
How Dangerous Is Recalled product administered From ALBUTEROL?
Of the 22 reports, 2 (9.1%) resulted in death.
Is Recalled product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALBUTEROL. However, 22 reports have been filed with the FAERS database.
What Other Side Effects Does ALBUTEROL Cause?
Dyspnoea (21,856)
Asthma (18,997)
Wrong technique in product usage process (17,114)
Wheezing (11,555)
Drug ineffective (11,057)
Device delivery system issue (9,509)
No adverse event (8,971)
Therapeutic product effect incomplete (8,496)
Cough (8,355)
Drug dose omission by device (8,162)
What Other Drugs Cause Recalled product administered?
RAMIPRIL (1,028)
LISINOPRIL (744)
PENICILLIN G BENZATHINE (500)
LEVOTHYROXINE (406)
HUMAN IMMUNOGLOBULIN G (382)
VARENICLINE (381)
VALSARTAN (267)
QUINAPRIL (243)
TRIAMCINOLONE ACETONIDE (222)
RANITIDINE (204)
Which ALBUTEROL Alternatives Have Lower Recalled product administered Risk?
ALBUTEROL vs ALBUTEROL\BUDESONIDE
ALBUTEROL vs ALBUTEROL\IPRATROPIUM
ALBUTEROL vs ALCAFTADINE
ALBUTEROL vs ALCOHOL
ALBUTEROL vs ALCOHOL\CHLORHEXIDINE