24,853 reports of this reaction
8.1% of all RANITIDINE reports
#1 most reported adverse reaction
BREAST CANCER is the #1 most commonly reported adverse reaction for RANITIDINE, manufactured by Ajanta Pharma USA Inc.. There are 24,853 FDA adverse event reports linking RANITIDINE to BREAST CANCER. This represents approximately 8.1% of all 308,223 adverse event reports for this drug.
RANITIDINE has an overall safety score of 95 out of 100. Patients taking RANITIDINE who experience breast cancer should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
BREAST CANCER is moderately reported among RANITIDINE users, representing a notable but not dominant share of adverse events.
In addition to breast cancer, the following adverse reactions have been reported for RANITIDINE:
The following drugs have also been linked to breast cancer in FDA adverse event reports:
BREAST CANCER has been reported as an adverse event in 24,853 FDA reports for RANITIDINE. This does not prove causation, but indicates an association observed in post-market surveillance data.
BREAST CANCER accounts for approximately 8.1% of all adverse event reports for RANITIDINE, making it one of the most commonly reported side effect.
If you experience breast cancer while taking RANITIDINE, contact your healthcare provider. They can evaluate whether the symptom is related to your medication and discuss potential adjustments to your treatment plan. Do not stop taking prescribed medication without consulting your doctor.