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Protonix IV

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Protonix I.V.

PATIENT INFORMATION

Inform patients that the most frequently occurring adverse reactions in US clinical trials for adults are headache, diarrhea, nausea, abdominal pain, vomiting, flatulence, dizziness, and arthralgia.

Patients should be instructed to inform their healthcare provider if they develop any unusual symptom, or if any known symptom persists or worsens. Patients should be instructed to inform their healthcare provider of any other medications they are currently taking, including over-the-counter medications, as well as allergies to any medications.

This product's label may have been updated. For current full prescribing information, please visit www.pfizer.com.

Last reviewed on RxList: 3/3/2014
This monograph has been modified to include the generic and brand name in many instances.

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Additional Protonix I.V. Information

Report Problems to the Food and Drug Administration

 

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.


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