Does DIETARY SUPPLEMENT\UBIDECARENONE Cause Condition aggravated? 19 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 19 reports of Condition aggravated have been filed in association with DIETARY SUPPLEMENT\UBIDECARENONE. This represents 16.4% of all adverse event reports for DIETARY SUPPLEMENT\UBIDECARENONE.
19
Reports of Condition aggravated with DIETARY SUPPLEMENT\UBIDECARENONE
16.4%
of all DIETARY SUPPLEMENT\UBIDECARENONE reports
2
Deaths
1
Hospitalizations
How Dangerous Is Condition aggravated From DIETARY SUPPLEMENT\UBIDECARENONE?
Of the 19 reports, 2 (10.5%) resulted in death, 1 (5.3%) required hospitalization.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DIETARY SUPPLEMENT\UBIDECARENONE. However, 19 reports have been filed with the FAERS database.
What Other Side Effects Does DIETARY SUPPLEMENT\UBIDECARENONE Cause?
Drug ineffective (30)
Cough (18)
Dyspnoea (17)
Pain (16)
Malaise (15)
Therapeutic product effect incomplete (15)
Wheezing (15)
Asthma (14)
Chest pain (14)
Throat clearing (14)
What Other Drugs Cause Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which DIETARY SUPPLEMENT\UBIDECARENONE Alternatives Have Lower Condition aggravated Risk?
DIETARY SUPPLEMENT\UBIDECARENONE vs DIFELIKEFALIN
DIETARY SUPPLEMENT\UBIDECARENONE vs DIFLUNISAL
DIETARY SUPPLEMENT\UBIDECARENONE vs DIFLUPREDNATE
DIETARY SUPPLEMENT\UBIDECARENONE vs DIGITOXIN
DIETARY SUPPLEMENT\UBIDECARENONE vs DIGOXIN