Does PENICILLIN G BENZATHINE Cause Recalled product administered? 500 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 500 reports of Recalled product administered have been filed in association with PENICILLIN G BENZATHINE (Lentocilin). This represents 44.1% of all adverse event reports for PENICILLIN G BENZATHINE.
500
Reports of Recalled product administered with PENICILLIN G BENZATHINE
44.1%
of all PENICILLIN G BENZATHINE reports
0
Deaths
2
Hospitalizations
How Dangerous Is Recalled product administered From PENICILLIN G BENZATHINE?
Of the 500 reports, 2 (0.4%) required hospitalization.
Is Recalled product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PENICILLIN G BENZATHINE. However, 500 reports have been filed with the FAERS database.
What Other Side Effects Does PENICILLIN G BENZATHINE Cause?
Drug hypersensitivity (109)
Embolia cutis medicamentosa (46)
Injection site pain (44)
Off label use (39)
Drug ineffective (31)
Foetal exposure during pregnancy (31)
Pain (31)
Rash (30)
Maternal exposure during pregnancy (21)
Premature baby (20)
What Other Drugs Cause Recalled product administered?
RAMIPRIL (1,028)
LISINOPRIL (744)
LEVOTHYROXINE (406)
HUMAN IMMUNOGLOBULIN G (382)
VARENICLINE (381)
VALSARTAN (267)
QUINAPRIL (243)
TRIAMCINOLONE ACETONIDE (222)
RANITIDINE (204)
LOSARTAN (141)
Which PENICILLIN G BENZATHINE Alternatives Have Lower Recalled product administered Risk?
PENICILLIN G BENZATHINE vs PENICILLIN G PROCAINE
PENICILLIN G BENZATHINE vs PENICILLIN V
PENICILLIN G BENZATHINE vs PENICILLIN V BENZATHINE
PENICILLIN G BENZATHINE vs PENTAMIDINE
PENICILLIN G BENZATHINE vs PENTAMIDINE ISETHIONATE