Does VARENICLINE Cause Recalled product? 12 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Recalled product have been filed in association with VARENICLINE (Varenicline). This represents 0.1% of all adverse event reports for VARENICLINE.
12
Reports of Recalled product with VARENICLINE
0.1%
of all VARENICLINE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Recalled product From VARENICLINE?
Of the 12 reports, and 1 (8.3%) were considered life-threatening.
Is Recalled product Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for VARENICLINE. However, 12 reports have been filed with the FAERS database.
What Other Side Effects Does VARENICLINE Cause?
Drug ineffective (2,625)
Nausea (2,232)
Abnormal dreams (1,656)
Malaise (986)
Depression (979)
Nightmare (978)
Feeling abnormal (864)
Insomnia (833)
Vomiting (777)
Drug hypersensitivity (729)
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 VARENICLINE Alternatives Have Lower Recalled product Risk?
VARENICLINE vs VARICELLA-ZOSTER VIRUS STRAIN OKA/MERCK LIVE ANTIGEN
VARENICLINE vs VASOPRESSIN
VARENICLINE vs VECTIBIX
VARENICLINE vs VECURONIUM
VARENICLINE vs VEDOLIZUMAB