7 reports of this reaction
2.5% of all SODIUM BICARBONATE, SODIUM CHLORIDE reports
#3 most reported adverse reaction
GASTROOESOPHAGEAL REFLUX DISEASE is the #3 most commonly reported adverse reaction for SODIUM BICARBONATE, SODIUM CHLORIDE, manufactured by CVS Pharmacy. There are 7 FDA adverse event reports linking SODIUM BICARBONATE, SODIUM CHLORIDE to GASTROOESOPHAGEAL REFLUX DISEASE. This represents approximately 2.5% of all 278 adverse event reports for this drug.
Patients taking SODIUM BICARBONATE, SODIUM CHLORIDE who experience gastrooesophageal reflux disease should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
GASTROOESOPHAGEAL REFLUX DISEASE is a less commonly reported adverse event for SODIUM BICARBONATE, SODIUM CHLORIDE, but still significant enough to appear in the safety profile.
In addition to gastrooesophageal reflux disease, the following adverse reactions have been reported for SODIUM BICARBONATE, SODIUM CHLORIDE:
The following drugs have also been linked to gastrooesophageal reflux disease in FDA adverse event reports:
GASTROOESOPHAGEAL REFLUX DISEASE has been reported as an adverse event in 7 FDA reports for SODIUM BICARBONATE, SODIUM CHLORIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
GASTROOESOPHAGEAL REFLUX DISEASE accounts for approximately 2.5% of all adverse event reports for SODIUM BICARBONATE, SODIUM CHLORIDE, making it one of the most commonly reported side effect.
If you experience gastrooesophageal reflux disease while taking SODIUM BICARBONATE, SODIUM CHLORIDE, 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.