DrugCite
Search

MINOXIDIL

Adverse Events
Drug Profile
Learn More
Reference
About Results
Comments

Minoxidil Adverse Events Reported to the FDA Over Time

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.

Most Common Minoxidil Adverse Events Reported to the FDA

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%)
Show More Show More
Drug Ineffective
37 (1.05%)
Heart Rate Increased
33 (.94%)
Alopecia
31 (.88%)
Myocardial Infarction
30 (.85%)
Pericardial Effusion
29 (.83%)
Swelling Face
29 (.83%)
Anxiety
27 (.77%)
Hypersensitivity
27 (.77%)
Malaise
27 (.77%)
Depression
26 (.74%)
Application Site Pruritus
24 (.68%)
Asthenia
24 (.68%)
Dermatitis Contact
24 (.68%)
Hypoaesthesia
24 (.68%)
Vomiting
24 (.68%)
Weight Increased
24 (.68%)
Eye Swelling
23 (.65%)
Pruritus
22 (.63%)
Psoriasis
22 (.63%)
Burning Sensation
21 (.6%)
Chest Discomfort
21 (.6%)
Insomnia
21 (.6%)
Skin Disorder
20 (.57%)
Underdose
18 (.51%)
Vision Blurred
18 (.51%)
Abdominal Pain
17 (.48%)
Chest Pain
17 (.48%)
Renal Failure Acute
17 (.48%)
Abdominal Distension
16 (.46%)
Auricular Swelling
16 (.46%)
Blister
16 (.46%)
Cardiac Disorder
16 (.46%)
Hair Growth Abnormal
16 (.46%)
Pleural Effusion
16 (.46%)
Tinnitus
16 (.46%)
Vertigo
16 (.46%)
Visual Impairment
16 (.46%)
Flushing
15 (.43%)
Hair Texture Abnormal
15 (.43%)
Pain
15 (.43%)
Chills
14 (.4%)
Herpes Zoster
14 (.4%)
Hyperhidrosis
14 (.4%)
Hypertrichosis
14 (.4%)
Paraesthesia
14 (.4%)
Accidental Exposure
13 (.37%)
Blood Pressure Decreased
13 (.37%)
Cerebrovascular Accident
13 (.37%)
Eczema
13 (.37%)
Skin Exfoliation
13 (.37%)
Urticaria
13 (.37%)
Condition Aggravated
12 (.34%)
Convulsion
12 (.34%)
Disturbance In Attention
12 (.34%)
Erythema
12 (.34%)
Fatigue
12 (.34%)
Feeling Abnormal
12 (.34%)
Fluid Retention
12 (.34%)
Heart Rate Irregular
12 (.34%)
Oedema
12 (.34%)
Scar
12 (.34%)
Viith Nerve Paralysis
12 (.34%)
Arrhythmia
11 (.31%)
Cardiac Failure Congestive
11 (.31%)
Death
11 (.31%)
Generalised Oedema
11 (.31%)
Visual Acuity Reduced
11 (.31%)
Acne
10 (.28%)
Arthralgia
10 (.28%)
Blood Pressure Fluctuation
10 (.28%)
Blood Pressure Inadequately Control...
10 (.28%)
Diplopia
10 (.28%)
Drug Hypersensitivity
10 (.28%)
Hair Colour Changes
10 (.28%)
Intraocular Pressure Increased
10 (.28%)
Swelling
10 (.28%)
Syncope
10 (.28%)
Wrong Technique In Drug Usage Proce...
10 (.28%)
Accidental Drug Intake By Child
9 (.26%)
Angina Pectoris
9 (.26%)
Atrial Fibrillation
9 (.26%)
Blood Creatinine Increased
9 (.26%)
Bone Pain
9 (.26%)
Depressed Mood
9 (.26%)
Dry Skin
9 (.26%)
Epistaxis
9 (.26%)
Hyponatraemia
9 (.26%)
Incorrect Route Of Drug Administrat...
9 (.26%)
Loss Of Consciousness
9 (.26%)
Pneumonia
9 (.26%)

ExportShare/Embed GraphExport Export Data

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.

Adverse Event Categories for Minoxidil

What are the most common Minoxidil adverse events reported to the FDA?

Show More Show More

ExportShare/Embed Graph Export Export Data

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.

Common Uses of Minoxidil According to Those Reporting Adverse Events

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
Show More Show More
Hair Growth Abnormal
25
Male Pattern Baldness
11
Accidental Exposure
6
Hypotrichosis
5
Blood Pressure Increased
5
Blood Pressure Management
4
Alopecia Areata
4
Hair Disorder
4
Blood Pressure Inadequately Control...
3
Female Pattern Baldness
2
Alcohol Use
2
Hirsutism
2
Malignant Hypertension
2
Cardiovascular Disorder
2
Ill-defined Disorder
2
Foetal Exposure During Pregnancy
2
Transplant Rejection
2
Rosacea
1
Drug Administration Error
1
Nephritis Autoimmune
1
Renovascular Hypertension
1
Overdose
1
Renal Hypertension
1
Alopecia Effluvium
1
Renal Transplant
1
Essential Hypertension
1
Drug Exposure During Pregnancy
1
Blood Pressure Abnormal
1
Prophylaxis
1
Gout
1
Hepatitis
1
Complex Regional Pain Syndrome
1

Drug Labels

LabelLabelerEffective
MinoxidilMutual Pharmaceutical Company, Inc.26-OCT-09
Minoxidilfor MenH E B16-FEB-10
MinoxidilNCS HealthCare of KY, Inc dba Vangard Labs02-JUN-10
MinoxidilState of Florida DOH Central Pharmacy07-JUN-10
MinoxidilWatson Laboratories, Inc.26-JUL-10
Minoxidilfor WomenWalgreen Company28-FEB-11
Minoxidilfor WomenPublix Super Markets Inc04-APR-11
MinoxidilH E B04-APR-11
MinoxidilREMEDYREPACK INC. 18-MAY-11
MinoxidilAmerican Health Packaging24-MAY-11
Minoxidilfor MenWalgreen Company20-JUL-11
MinoxidilWalgreen Company08-AUG-11
Up And Up MinoxidilTarget Corporation12-AUG-11
Simply Right Minoxidilextra StrengthSam's West Inc23-AUG-11
Minoxidilregular StrengthH E B30-AUG-11
Minoxidilregular StrengthH E B30-AUG-11
Hair Regrowth Treatment For MenActavis Mid Atlantic LLC12-SEP-11
Hair Regrowth TreatmentActavis Mid Atlantic LLC20-OCT-11
MinoxidilHi-Tech Pharmacal Co., Inc.16-NOV-11
MinoxidilHi-Tech Pharmacal Co., Inc.16-NOV-11
MinoxidilPublix Super Markets Inc28-NOV-11
Hair Regrowth Treatment For WomenPremier Value01-JAN-12
MinoxidilPhysicians Total Care, Inc.04-MAR-12
Minoxidil For WomenRite Aid15-MAR-12
Minoxidil For WomenCVS15-MAR-12
Kirkland Signature MinoxidilCostco Wholesale Company01-JUN-12
Up And Up MinoxidilTarget Corporation20-JUN-12
Mens Rogaine Unscented FormulaJohnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc.01-AUG-12
MinoxidilWalgreen Company14-AUG-12
MinoxidilPhysicians Total Care, Inc.02-OCT-12
MinoxidilPar Pharmaceutical Inc15-JAN-13
MinoxidilWalgreen Company21-JAN-13
Kirkland Signature MinoxidilCostco Wholesale Company21-JAN-13
Up And Up MinoxidilTarget Corporation21-JAN-13
MinoxidilH E B24-JAN-13
Simply Right MinoxidilSam's West Inc25-JAN-13
MinoxidilREMEDYREPACK INC. 26-FEB-13
MinoxidilREMEDYREPACK INC. 20-MAR-13

Minoxidil Case Reports

What Minoxidil safety concerns are being reported by doctors and researchers in the medical literature?

Powered by Google

About Results

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.

Comments

Share your experience with Minoxidil.