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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does RANITIDINE Cause Recalled product? 13 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 13 reports of Recalled product have been filed in association with RANITIDINE (Ranitidine). This represents 0.0% of all adverse event reports for RANITIDINE.

13
Reports of Recalled product with RANITIDINE
0.0%
of all RANITIDINE reports
0
Deaths
1
Hospitalizations

How Dangerous Is Recalled product From RANITIDINE?

Of the 13 reports, 1 (7.7%) required hospitalization, and 1 (7.7%) 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 RANITIDINE. However, 13 reports have been filed with the FAERS database.

What Other Side Effects Does RANITIDINE Cause?

Prostate cancer (60,641) Breast cancer (45,666) Colorectal cancer (45,528) Bladder cancer (41,984) Renal cancer (40,791) Oesophageal carcinoma (26,229) Gastric cancer (18,927) Hepatic cancer (17,818) Pancreatic carcinoma (15,752) Lung neoplasm malignant (15,214)

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 RANITIDINE Alternatives Have Lower Recalled product Risk?

RANITIDINE vs RANITIDINE\RANITIDINE RANITIDINE vs RANOLAZINE RANITIDINE vs RAPAMUNE RANITIDINE vs RASAGILINE RANITIDINE vs RASBURICASE

Related Pages

RANITIDINE Full Profile All Recalled product Reports All Drugs Causing Recalled product RANITIDINE Demographics