How are Minoxidil adverse event reports trending over time?
This graph shows volume of adverse events submitted to the FDA by quarter for Minoxidil, as well as related generic and/or brandname drugs containing the same primary active ingredients. Adverse events are counted if Minoxidil is flagged as the suspect drug causing the adverse event.
What are the most common Minoxidil adverse events reported to the FDA?
Dizziness | 65 (1.85%) |
Wrong Drug Administered | 57 (1.62%) |
Dyspnoea | 56 (1.59%) |
Nausea | 48 (1.37%) |
Tachycardia | 48 (1.37%) |
Headache | 47 (1.34%) |
Blood Pressure Increased | 44 (1.25%) |
Oedema Peripheral | 44 (1.25%) |
Hypertension | 43 (1.22%) |
Hypotension | 42 (1.2%) |
Palpitations | 38 (1.08%) |
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This graph shows the top adverse events submitted to the FDA for Minoxidil, 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 Minoxidil 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 Minoxidil adverse events reported to the FDA?
Epidermal And Dermal Conditions | 307 (8.74%) |
Neurological | 175 (4.98%) |
Medication Errors | 145 (4.13%) |
Cardiac And Vascular Investigations | 134 (3.82%) |
Gastrointestinal Signs | 114 (3.25%) |
Skin Appendage Conditions | 113 (3.22%) |
Cardiac Arrhythmias | 101 (2.88%) |
Administration Site Reactions | 90 (2.56%) |
Respiratory | 89 (2.53%) |
Vision | 68 (1.94%) |
Decreased And Nonspecific Blood Pre... | 66 (1.88%) |
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This graph shows the top categories of adverse events submitted to the FDA for Minoxidil, 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 Minoxidil 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 Minoxidil, according to those reporting adverse events to the FDA?
Alopecia | 253 |
Hypertension | 239 |
Product Used For Unknown Indication | 143 |
Drug Use For Unknown Indication | 84 |
Androgenetic Alopecia | 35 |
Blood Pressure | 25 |
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Label | Labeler | Effective |
---|---|---|
Minoxidil | Mutual Pharmaceutical Company, Inc. | 26-OCT-09 |
Minoxidilfor Men | H E B | 16-FEB-10 |
Minoxidil | NCS HealthCare of KY, Inc dba Vangard Labs | 02-JUN-10 |
Minoxidil | State of Florida DOH Central Pharmacy | 07-JUN-10 |
Minoxidil | Watson Laboratories, Inc. | 26-JUL-10 |
Minoxidilfor Women | Walgreen Company | 28-FEB-11 |
Minoxidilfor Women | Publix Super Markets Inc | 04-APR-11 |
Minoxidil | H E B | 04-APR-11 |
Minoxidil | REMEDYREPACK INC. | 18-MAY-11 |
Minoxidil | American Health Packaging | 24-MAY-11 |
Minoxidilfor Men | Walgreen Company | 20-JUL-11 |
Minoxidil | Walgreen Company | 08-AUG-11 |
Up And Up Minoxidil | Target Corporation | 12-AUG-11 |
Simply Right Minoxidilextra Strength | Sam's West Inc | 23-AUG-11 |
Minoxidilregular Strength | H E B | 30-AUG-11 |
Minoxidilregular Strength | H E B | 30-AUG-11 |
Hair Regrowth Treatment For Men | Actavis Mid Atlantic LLC | 12-SEP-11 |
Hair Regrowth Treatment | Actavis Mid Atlantic LLC | 20-OCT-11 |
Minoxidil | Hi-Tech Pharmacal Co., Inc. | 16-NOV-11 |
Minoxidil | Hi-Tech Pharmacal Co., Inc. | 16-NOV-11 |
Minoxidil | Publix Super Markets Inc | 28-NOV-11 |
Hair Regrowth Treatment For Women | Premier Value | 01-JAN-12 |
Minoxidil | Physicians Total Care, Inc. | 04-MAR-12 |
Minoxidil For Women | Rite Aid | 15-MAR-12 |
Minoxidil For Women | CVS | 15-MAR-12 |
Kirkland Signature Minoxidil | Costco Wholesale Company | 01-JUN-12 |
Up And Up Minoxidil | Target Corporation | 20-JUN-12 |
Mens Rogaine Unscented Formula | Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc. | 01-AUG-12 |
Minoxidil | Walgreen Company | 14-AUG-12 |
Minoxidil | Physicians Total Care, Inc. | 02-OCT-12 |
Minoxidil | Par Pharmaceutical Inc | 15-JAN-13 |
Minoxidil | Walgreen Company | 21-JAN-13 |
Kirkland Signature Minoxidil | Costco Wholesale Company | 21-JAN-13 |
Up And Up Minoxidil | Target Corporation | 21-JAN-13 |
Minoxidil | H E B | 24-JAN-13 |
Simply Right Minoxidil | Sam's West Inc | 25-JAN-13 |
Minoxidil | REMEDYREPACK INC. | 26-FEB-13 |
Minoxidil | REMEDYREPACK INC. | 20-MAR-13 |
What Minoxidil safety concerns are being reported by doctors and researchers in the medical literature?
This report contains aggregated drug side effects and adverse events for Minoxidil. 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.
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