Does VARENICLINE Cause Recalled product administered? 381 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 381 reports of Recalled product administered have been filed in association with VARENICLINE (Varenicline). This represents 1.9% of all adverse event reports for VARENICLINE.
381
Reports of Recalled product administered with VARENICLINE
1.9%
of all VARENICLINE reports
0
Deaths
28
Hospitalizations
How Dangerous Is Recalled product administered From VARENICLINE?
Of the 381 reports, 28 (7.3%) required hospitalization, and 5 (1.3%) were considered life-threatening.
Is Recalled product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for VARENICLINE. However, 381 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 administered?
RAMIPRIL (1,028)
LISINOPRIL (744)
PENICILLIN G BENZATHINE (500)
LEVOTHYROXINE (406)
HUMAN IMMUNOGLOBULIN G (382)
VALSARTAN (267)
QUINAPRIL (243)
TRIAMCINOLONE ACETONIDE (222)
RANITIDINE (204)
LOSARTAN (141)
Which VARENICLINE Alternatives Have Lower Recalled product administered Risk?
VARENICLINE vs VARICELLA-ZOSTER VIRUS STRAIN OKA/MERCK LIVE ANTIGEN
VARENICLINE vs VASOPRESSIN
VARENICLINE vs VECTIBIX
VARENICLINE vs VECURONIUM
VARENICLINE vs VEDOLIZUMAB