PANTOPRAZOLE SODIUM FDA MedWatch Voluntary U.S. Reports Summary

These tables and charts are created from 1,142 U.S. reports for PANTOPRAZOLE SODIUM (PANTOPRAZOLE SODIUM) voluntarily reported by individuals directly to the FDA via the MedWatch Reporting System from 2004 through July 30, 2026. Events listed on this page represent serious and often rare adverse events reported to the FDA, and often do not represent typical side effects for the medication. Find common side effects on the most recent official drug label.

For a summary of adverse events including mandatory reports submitted by pharmaceutical companies (all countries and all reporter types) to the FAERS database, View FDA FAERS PANTOPRAZOLE SODIUM Report.

Top Adverse Events Reported with PANTOPRAZOLE SODIUM (from U.S. FDA Medwatch Reports)

	Side Effect	# of FDA Reports
1	DEATH	122
2	NAUSEA	66
3	DIARRHEA	60
4	SHORTNESS OF BREATH	60
5	DIZZINESS	49
6	DISEASE PROGRESSION	48
7	DRUG INEFFECTIVE	41
8	HOSPITALIZATION	41
9	FATIGUE	40
10	HEADACHE	40
11	THERAPY INTERRUPTED	40
12	VOMITING	35
13	LACK OF STRENGTH AND ENERGY (ASTHENIA)	32
14	JOINT PAIN	31
15	THERAPY CESSATION	31
16	HOSPICE CARE	29
17	PRODUCT PACKAGING CONFUSION	27
18	PAIN	24
19	INSOMNIA	23
20	ITCHING	23
21	RASH	21
22	ABDOMINAL PAIN	20
23	ABDOMINAL PAIN UPPER	20
24	GASTROOESOPHAGEAL REFLUX DISEASE	19
25	PRODUCT DISPENSING ERROR	19

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PANTOPRAZOLE SODIUM Total Medwatch Safety Reports by Patient Sex

Male	Female	Unknown	Total
411	628	103	1,142

Medwatch Reporter Type	Count
Consumer	335
Physician	118
Pharmacist	240
Other Health Professional	257

Top Indications

Product used for unknown indication
Gastrooesophageal reflux disease
Chronic gastritis
Prophylaxis
Barrett's oesophagus

Type of Outcome Reported
Serious: 704
Not Serious: 438
Note: A serious outcome means the adverse event resulted in death, a life threatening condition, hospitalization, disability, congenital anomaly, or other serious condition.

Suspected Role
Primary Suspect: 1139
Concomitant Drugs: 962
Note: A single MedWatch report can list more than one drug. This summary includes PANTOPRAZOLE SODIUM identified as the suspect drug or as a concomitantly taken drug.

FDA Safety-Related Labeling Changes

PROTONIX (PANTOPRAZOLE SODIUM) Rx Drug:
FDA Safety-related Labeling Changes

PROTONIX IV (PANTOPRAZOLE SODIUM) Rx Drug:
FDA Safety-related Labeling Changes

Have experience (good or bad) with PROTONIX IV? Rate PROTONIX IV at Ask a Patient.

For serious adverse events, report them to the FDA by contacting the drug manufacturer or report directly through the MedWatch voluntary reporting form.

NOTES

This report, created by AskaPatient.com, is derived from U.S. drug-related adverse event cases that were reported directly to the FDA using the voluntary MedWatch online or paper reporting system. MedWatch is the voluntary FDA system for consumers, physicians, and others to directly report adverse reactions. The Medwatch initiative was launched in 1993 as a voluntary reporting program for consumers, physicians and other healthcare practitioners.

After processing the received forms, the FDA adds the MedWatch reports to the FDA Adverse Events Reporting System(or FAERS database.) Click here for the complete FAERS report summary, which includes mandatory reports submitted by pharmaceutical companies (worldwide) combined with the MedWatch reports. MedWatch Reports only represent about 5% of the FAERS database. For more, read "Does the FDA's Rapidly Growing Database of Adverse Events Improve Drug Safety?"

The data in this report was obtained from Open FDA. Data was last updated to include reports through January 27, 2026. The reactions, side effects, or "adverse events," represent up to the 20 most frequently occuring events in the database for a drug related to the event.

Open FDA states that it only includes the most recent version of a case report. It also adds the disclaimer: "Do not rely on Open FDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated."

FDA uses the "MedDRA" classification system to describe reported adverse reactions. MedDRA is a standardized medical terminology that facilitates sharing of regulatory information internationally. In some cases, "patient friendly" terms for the layman designated by MedDRA have been substituted for medical jargon. Please contact us with questions about this report.