Does OXCARBAZEPINE Cause Recalled product? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Recalled product have been filed in association with OXCARBAZEPINE (OXCARBAZEPINE). This represents 0.1% of all adverse event reports for OXCARBAZEPINE.
6
Reports of Recalled product with OXCARBAZEPINE
0.1%
of all OXCARBAZEPINE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Recalled product From OXCARBAZEPINE?
Of the 6 reports.
Is Recalled product Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for OXCARBAZEPINE. However, 6 reports have been filed with the FAERS database.
What Other Side Effects Does OXCARBAZEPINE Cause?
Seizure (1,525)
Drug ineffective (1,498)
Off label use (751)
Hyponatraemia (708)
Somnolence (634)
Dizziness (558)
Fatigue (551)
Epilepsy (509)
Headache (505)
Asthenia (429)
What Other Drugs Cause Recalled product?
PARATHYROID HORMONE (900)
ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT (80)
CALCITRIOL (68)
CALCIUM (66)
REMDESIVIR (36)
LEVOTHYROXINE\LIOTHYRONINE (34)
TESTOSTERONE (32)
VALSARTAN (32)
CHLORHEXIDINE (28)
ALCOHOL (26)
Which OXCARBAZEPINE Alternatives Have Lower Recalled product Risk?
OXCARBAZEPINE vs OXITRIPTAN
OXCARBAZEPINE vs OXOMEMAZINE
OXCARBAZEPINE vs OXY TAB
OXCARBAZEPINE vs OXYBATE
OXCARBAZEPINE vs OXYBUTYNIN