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Rolaids Regular Strength Side Effects

Generic name: calcium carbonate / magnesium hydroxide

Medically reviewed by Drugs.com. Last updated on May 7, 2024.

Note: This document provides detailed information about Rolaids Regular Strength Side Effects associated with calcium carbonate / magnesium hydroxide. Some dosage forms listed on this page may not apply specifically to the brand name Rolaids Regular Strength.

Applies to calcium carbonate / magnesium hydroxide: oral tablet chewable.

Important warnings This medicine can cause some serious health issues

Follow all directions on the label and package.

Use exactly as directed.

Get emergency medical help if you have signs of an allergic reaction: hives, difficult breathing, swelling of your face, lips, tongue, or throat.

Stop using this medicine and call your doctor at once if you have symptoms of high calcium or magnesium levels in your blood:

Common side effects may include:

This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects.

For healthcare professionals

Applies to calcium carbonate/magnesium hydroxide: oral capsule, oral suspension, oral tablet chewable.

General adverse events

The manufacturer has not provided adverse event information.[Ref]

See also:

References

1. (2004) "Product Information. Rolaids (calcium carbonate-magnesium hydroxide)." Pfizer U.S. Pharmaceuticals Group

2. (2004) "Product Information. Rolaids Extra Strength (calcium carbonate-magnesium hydroxide)." Pfizer U.S. Pharmaceuticals Group

3. Cerner Multum, Inc. "Australian Product Information."

4. (2019) "Product Information. Rolaids Soft Chew (calcium carbonate)." Johnson and Johnson/McNeil Consumer

Further information

Rolaids Regular Strength side effects can vary depending on the individual. Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Note: Medication side effects may be underreported. If you are experiencing side effects that are not listed, submit a report to the FDA by following this guide.