VIAGRA FDA MedWatch Direct Reports Summary

These tables and charts are created from 394 voluntary U.S. reports for VIAGRA (SILDENAFIL CITRATE) reported by individuals to the FDA via the MedWatch Reporting System from 2004 through April 28, 2026.

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 VIAGRA Report.

Top Adverse Effects Associated with VIAGRA (from U.S. FDA Medwatch Reports)

	Side Effect	# of FDA Reports
1	DRUG INEFFECTIVE	27
2	HEADACHE	21
3	DIZZINESS	19
4	NAUSEA	18
5	JOINT PAIN	16
6	FATIGUE	16
7	DEATH	14
8	DIARRHEA	14
9	SHORTNESS OF BREATH	14
10	PAIN	12
11	ERECTILE DYSFUNCTION	11
12	VISION BLURRED	11
13	HEART ATTACK (MYOCARDIAL INFARCTION)	9
14	ABDOMINAL PAIN	8
15	LACK OF STRENGTH AND ENERGY (ASTHENIA)	8
16	INFLUENZA LIKE ILLNESS	8
17	LOSS OF CONSCIOUSNESS	8
18	MUSCLE PAIN	8
19	PRODUCT SUBSTITUTION ISSUE	8
20	THERAPY CESSATION	8
21	VOMITING	8
22	ANXIETY	7
23	CONDITION AGGRAVATED	7
24	COUGH	7
25	DISEASE PROGRESSION	7

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VIAGRA Total Medwatch Safety Reports by Patient Sex

Male	Female	Unknown	Total
363	17	14	394

Medwatch Reporter Type	Count
Consumer	125
Physician	25
Pharmacist	79
Other Health Professional	56

Top Indications

Erectile dysfunction
Product used for unknown indication
Pulmonary hypertension

Type of Outcome Reported
Serious: 271
Not Serious: 123
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: 394
Concomitant Drugs: 302
Note: A single MedWatch report can list more than one drug. This summary includes VIAGRA identified as the suspect drug or as a concomitantly taken drug.

FDA Safety-Related Labeling Changes

VIAGRA (SILDENAFIL CITRATE) Rx Drug:
FDA Safety-related Labeling Changes

Have experience (good or bad) with VIAGRA? Rate VIAGRA 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.