How are Hydralazine adverse event reports trending over time?
This graph shows volume of adverse events submitted to the FDA by quarter for Hydralazine, as well as related generic and/or brandname drugs containing the same primary active ingredients. Adverse events are counted if Hydralazine is flagged as the suspect drug causing the adverse event.
What are the most common Hydralazine adverse events reported to the FDA?
Completed Suicide | 74 (2.01%) |
Drug Exposure During Pregnancy | 72 (1.95%) |
Blood Pressure Increased | 70 (1.9%) |
Hypertension | 57 (1.54%) |
Hypotension | 55 (1.49%) |
Premature Baby | 50 (1.36%) |
Caesarean Section | 49 (1.33%) |
Dizziness | 47 (1.27%) |
Headache | 41 (1.11%) |
Oedema Peripheral | 40 (1.08%) |
Drug Ineffective | 38 (1.03%) |
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This graph shows the top adverse events submitted to the FDA for Hydralazine, as well as related generic and/or brandname drugs containing the same primary active ingredients, from Q1 2004 to Q3 2012. Adverse events are counted if Hydralazine is flagged as a suspect drug causing the adverse event. For each adverse event listed, percent (%) represents percentage of the adverse event to all adverse events reported for the drug. Percent does not represent a rate related to drug utilization.
What are the most common Hydralazine adverse events reported to the FDA?
Neurological | 201 (5.45%) |
Cardiac And Vascular Investigations | 155 (4.2%) |
Cardiac Arrhythmias | 141 (3.82%) |
Respiratory | 118 (3.2%) |
Medication Errors | 112 (3.04%) |
Epidermal And Dermal Conditions | 109 (2.95%) |
Chemical Injury And Poisoning | 99 (2.68%) |
Decreased And Nonspecific Blood Pre... | 87 (2.36%) |
Renal Disorders | 87 (2.36%) |
Suicidal And Self-injurious Behavio... | 75 (2.03%) |
Gastrointestinal Signs | 70 (1.9%) |
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This graph shows the top categories of adverse events submitted to the FDA for Hydralazine, as well as related generic and/or brandname drugs containing the same primary active ingredients, from Q1 2004 to Q3 2012. Adverse events are counted if Hydralazine is flagged as a suspect drug causing the adverse event. For each adverse event listed, percent (%) represents percentage of the adverse event to all adverse events reported for the drug. Percent does not represent a rate related to drug utilization.
Why are people taking Hydralazine, according to those reporting adverse events to the FDA?
Hypertension | 706 |
Drug Use For Unknown Indication | 352 |
Product Used For Unknown Indication | 348 |
Blood Pressure | 76 |
Cardiac Disorder | 38 |
Blood Pressure Abnormal | 28 |
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Label | Labeler | Effective |
---|---|---|
Hydralazine Hydrochloride | Mylan Pharmaceuticals Inc. | 08-JAN-09 |
Hydralazine Hydrochloride | Glenmark Generics Inc., USA | 03-JUN-09 |
Hydralazine | McKesson Packaging Services Business Unit of McKesson Corporation | 09-NOV-09 |
Hydralazine Hydrochloride | General Injectables & Vaccines, Inc | 03-SEP-10 |
Hydralazine Hydrochloride | UDL Laboratories, Inc. | 10-SEP-10 |
Hydralazine Hydrochloride | REMEDYREPACK INC. | 18-NOV-10 |
Hydralazine Hydrochloride | Rebel Distributors Corp | 17-JAN-11 |
Hydralazine Hydrochloride | APP Pharmaceuticals, LLC | 28-JAN-11 |
Hydralazine Hydrochloride | Heritage Pharmaceuticals Inc | 15-MAR-11 |
Hydralazine Hydrochloride | PD-Rx Pharmaceuticals, Inc. | 15-MAR-11 |
Hydralazine Hydrochloride | REMEDYREPACK INC. | 19-APR-11 |
Hydralazine Hydrochloride | REMEDYREPACK INC. | 28-APR-11 |
Hydralazine Hydrochloride | Cardinal Health | 06-MAY-11 |
Hydralazine Hydrochloride | Cardinal Health | 24-MAY-11 |
Hydralazine Hydrochloride | Cardinal Health | 24-MAY-11 |
Hydralazine Hydrochloride | Physicians Total Care, Inc. | 16-JUN-11 |
Hydralazine Hydrochloride | Golden State Medical Supply, Inc. | 01-JUL-11 |
Hydralazine Hydrochloride | Camber Pharmaceuticals | 17-AUG-11 |
Hydralazine Hydrochloride | American Health Packaging | 22-SEP-11 |
Hydralazine Hydrochloride | American Regent, Inc. | 09-OCT-11 |
Hydralazine Hydrochloride | General Injectables & Vaccines, Inc | 18-OCT-11 |
Hydralazine Hydrochloride | NCS HealthCare of KY, Inc dba Vangard Labs | 04-NOV-11 |
Hydralazine Hydrochloride | REMEDYREPACK INC. | 17-NOV-11 |
Hydralazine Hydrochloride | AMERISOURCEBERGEN DRUG CORPORATION | 08-DEC-11 |
Hydralazine Hydrochloride | REMEDYREPACK INC. | 09-DEC-11 |
Hydralazine Hydrochloride | McKesson Contract Packaging | 14-DEC-11 |
Hydralazine Hydrochloride | APP Pharmaceuticals, LLC | 20-JAN-12 |
Hydralazine Hydrochloride | Par Pharmaceutical, Inc. | 01-MAR-12 |
Hydralazine Hydrochloride | Akorn, Inc. | 23-MAR-12 |
Hydralazine Hydrochloride | Cardinal Health | 19-APR-12 |
Hydralazine Hydrochloride | Cardinal Health | 19-APR-12 |
Hydralazine Hydrochloride | Cardinal Health | 27-APR-12 |
Hydralazine Hydrochloride | Cardinal Health | 27-APR-12 |
Hydralazine Hydrochloride | Physicians Total Care, Inc. | 20-JUN-12 |
Bidil | Arbor Pharmaceuticals | 17-AUG-12 |
Hydralazine Hydrochloride | Pliva Inc. | 17-DEC-12 |
Hydralazine Hydrochloride | Akorn, Inc. | 21-FEB-13 |
Bidil | Arbor Pharmaceuticals, Inc. | 01-MAR-13 |
Hydralazine Hydrochloride | Ascend Laboratories, LLC | 04-MAR-13 |
Hydralazine Hydrochloride | REMEDYREPACK INC. | 18-MAR-13 |
Hydralazine | Cardinal Health | 09-APR-13 |
Hydralazine Hydrochloride | Goldline Laboratories, Inc. | 11-APR-13 |
Hydralazine Hydrochloride | REMEDYREPACK INC. | 02-MAY-13 |
What Hydralazine safety concerns are being reported by doctors and researchers in the medical literature?
This report contains aggregated drug side effects and adverse events for Hydralazine. The data has been pulled from the United States Food and Drug Administration's (US FDA) Adverse Event Reporting System (AERS), a database containing more than 4,000,000 adverse event reports.
DrugCite expands your query using the Unified Medical Language System (UMLS) to include generic drugs and primary active ingredients. While the core of DrugCite's advanced drug filtering algorithm is based on the industry standard UMLS, DrugCite's proprietary filtering system also includes dozens of additional steps to reconcile malformed drug names in the FDA's data.
DrugCite only counts a drug if the submitter of the adverse event indicates that the drug is suspected to have caused the adverse event.
Depending on how the data is aggregated, different counts may occur. When someone submits an adverse event to the FDA, the submitter can attribute multiple adverse events to one or more drugs. For example, an individual taking Paxil could submit the adverse events "anxiety" and "suicidal ideation" for the same individual safety report (ISR). This means when DrugCite aggregates by adverse event, two distinct adverse events are counted in the adverse event graph; once for "anxiety" and again for "suicidal ideation". However, when DrugCite aggregates by individual safety reports irrespective of the details of the adverse events contained within the safety report, the report is only counted once.
Share your experience with Hydralazine.