Does AZITHROMYCIN ANHYDROUS Cause Product dose omission? 14 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Product dose omission have been filed in association with AZITHROMYCIN ANHYDROUS. This represents 0.1% of all adverse event reports for AZITHROMYCIN ANHYDROUS.
14
Reports of Product dose omission with AZITHROMYCIN ANHYDROUS
0.1%
of all AZITHROMYCIN ANHYDROUS reports
1
Deaths
5
Hospitalizations
How Dangerous Is Product dose omission From AZITHROMYCIN ANHYDROUS?
Of the 14 reports, 1 (7.1%) resulted in death, 5 (35.7%) required hospitalization.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for AZITHROMYCIN ANHYDROUS. However, 14 reports have been filed with the FAERS database.
What Other Side Effects Does AZITHROMYCIN ANHYDROUS Cause?
Off label use (3,288)
Drug ineffective (1,587)
Drug hypersensitivity (1,355)
Dyspnoea (947)
Nausea (727)
Diarrhoea (696)
Asthma (668)
Product use in unapproved indication (639)
Condition aggravated (621)
Cough (580)
What Other Drugs Cause Product dose omission?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which AZITHROMYCIN ANHYDROUS Alternatives Have Lower Product dose omission Risk?
AZITHROMYCIN ANHYDROUS vs AZITHROMYCIN OR METHOTREXATE
AZITHROMYCIN ANHYDROUS vs AZOSEMIDE
AZITHROMYCIN ANHYDROUS vs AZTREONAM
AZITHROMYCIN ANHYDROUS vs AZTREONAM LYSINE
AZITHROMYCIN ANHYDROUS vs BACILLUS CALMETTE-GUERIN ANTIGEN, UNSPECIFIED SUBSTRAIN