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FINASTERIDE

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Finasteride Adverse Events Reported to the FDA Over Time

How are Finasteride adverse event reports trending over time?

This graph shows volume of adverse events submitted to the FDA by quarter for Finasteride, as well as related generic and/or brandname drugs containing the same primary active ingredients. Adverse events are counted if Finasteride is flagged as the suspect drug causing the adverse event.

Most Common Finasteride Adverse Events Reported to the FDA

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

Erectile Dysfunction
87 (3.31%)
Depression
64 (2.43%)
Anxiety
51 (1.94%)
Fatigue
50 (1.9%)
Gynaecomastia
48 (1.82%)
Dizziness
38 (1.44%)
Libido Decreased
38 (1.44%)
Loss Of Libido
35 (1.33%)
Loss Of Consciousness
32 (1.22%)
Wrong Technique In Drug Usage Proce...
32 (1.22%)
Disturbance In Attention
29 (1.1%)
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Testicular Pain
27 (1.03%)
Drug Ineffective
26 (.99%)
Asthenia
24 (.91%)
Myalgia
24 (.91%)
Arthralgia
23 (.87%)
Penis Disorder
23 (.87%)
Insomnia
22 (.84%)
Haematuria
21 (.8%)
Ventricular Extrasystoles
21 (.8%)
Hyperthyroidism
20 (.76%)
Sexual Dysfunction
20 (.76%)
Intentional Drug Misuse
19 (.72%)
Aggression
18 (.68%)
Drug Interaction
17 (.65%)
Suicidal Ideation
17 (.65%)
Urine Flow Decreased
17 (.65%)
Product Substitution Issue
16 (.61%)
Blood Testosterone Decreased
15 (.57%)
Dyspnoea
14 (.53%)
Rash
14 (.53%)
Atrioventricular Block First Degree
13 (.49%)
Ejaculation Failure
13 (.49%)
Fall
13 (.49%)
Muscle Spasms
13 (.49%)
Penile Size Reduced
13 (.49%)
Semen Volume Decreased
13 (.49%)
Accidental Exposure
12 (.46%)
Alanine Aminotransferase Increased
12 (.46%)
Amnesia
12 (.46%)
Anhedonia
12 (.46%)
Dysgeusia
12 (.46%)
Muscle Atrophy
12 (.46%)
Palpitations
12 (.46%)
Prostatitis
12 (.46%)
Tremor
12 (.46%)
Apathy
11 (.42%)
Cerebrovascular Accident
11 (.42%)
Drug Dispensing Error
11 (.42%)
Drug Prescribing Error
11 (.42%)
Pain
11 (.42%)
Panic Attack
11 (.42%)
Product Quality Issue
11 (.42%)
Dark Circles Under Eyes
10 (.38%)
Diarrhoea
10 (.38%)
Dysuria
10 (.38%)
Emotional Disorder
10 (.38%)
Hallucination
10 (.38%)
Mental Disorder
10 (.38%)
Self Esteem Decreased
10 (.38%)
Testicular Atrophy
10 (.38%)
Urinary Retention
10 (.38%)
Cognitive Disorder
9 (.34%)
Emotional Distress
9 (.34%)
Flatulence
9 (.34%)
Hyperhidrosis
9 (.34%)
Impaired Work Ability
9 (.34%)
Memory Impairment
9 (.34%)
Mood Swings
9 (.34%)
Oedema Peripheral
9 (.34%)
Prostatic Specific Antigen Increase...
9 (.34%)
Psychiatric Symptom
9 (.34%)
Skin Disorder
9 (.34%)
Wrong Drug Administered
9 (.34%)
Anger
8 (.3%)
Back Pain
8 (.3%)
Blood Glucose Increased
8 (.3%)
Coordination Abnormal
8 (.3%)
Dizziness Postural
8 (.3%)
Dry Skin
8 (.3%)
Feeling Abnormal
8 (.3%)
Floppy Iris Syndrome
8 (.3%)
Homicide
8 (.3%)
Musculoskeletal Pain
8 (.3%)
Organic Erectile Dysfunction
8 (.3%)
Paraesthesia
8 (.3%)
Prostate Cancer
8 (.3%)
Pruritus
8 (.3%)
Rhinorrhoea
8 (.3%)
Testicular Swelling
8 (.3%)
Thrombocytopenia
8 (.3%)
Azoospermia
7 (.27%)
Blood Alkaline Phosphatase Increase...
7 (.27%)
Depressed Mood
7 (.27%)
Gait Disturbance
7 (.27%)
Hormone Level Abnormal
7 (.27%)
Liver Function Test Abnormal
7 (.27%)
Muscle Disorder
7 (.27%)
Nocturia
7 (.27%)
Pain In Extremity
7 (.27%)
Skin Atrophy
7 (.27%)

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This graph shows the top adverse events submitted to the FDA for Finasteride, 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 Finasteride 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 Finasteride

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

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This graph shows the top categories of adverse events submitted to the FDA for Finasteride, 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 Finasteride 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 Finasteride According to Those Reporting Adverse Events

Why are people taking Finasteride, according to those reporting adverse events to the FDA?

Benign Prostatic Hyperplasia
347
Product Used For Unknown Indication
302
Prostatic Disorder
220
Prostatomegaly
137
Alopecia
136
Drug Use For Unknown Indication
113
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Androgenetic Alopecia
43
Prostate Cancer
30
Prostatism
16
Urinary Retention
13
Dysuria
10
Hypertension
9
Urinary Tract Disorder
9
Male Pattern Baldness
9
Benign Neoplasm Of Prostate
8
Prophylaxis
8
Pollakiuria
8
Prostatic Adenoma
7
Prostatitis
7
Prostate Examination Abnormal
7
Oedema
6
Bladder Disorder
6
Hair Growth Abnormal
6
Ill-defined Disorder
5
Nocturia
4
Prostatic Specific Antigen Increase...
3
Micturition Urgency
3
Hair Transplant
3
Blood Testosterone Increased
3
Accidental Exposure
2
Acne
2
Maternal Exposure During Pregnancy
2
Swelling
2
Blood Pressure Increased
2
Urinary Incontinence
2
Prostatic Specific Antigen Abnormal
2
Haemorrhage
1
Supplementation Therapy
1
Hormone Level Abnormal
1
Drug Exposure During Pregnancy
1
Blood Potassium
1
Tourettes Disorder
1
Fluid Retention
1
Prostate Infection
1
Adverse Drug Reaction
1
Blood Cholesterol Increased
1
Dihydrotestosterone Increased
1
Prostate Induration
1
Incontinence
1
Off Label Use
1
Obstructive Uropathy
1

Drug Labels

LabelLabelerEffective
Finasteride AvPAK15-JUL-10
FinasterideCamber Pharmaceuticals Inc.15-JUL-10
FinasteridePhysicians Total Care, Inc.31-AUG-10
FinasterideMcKesson Packaging Services Business Unit of McKesson Corporation16-NOV-10
FinasterideActavis Totowa LLC30-NOV-10
FinasterideMylan Pharmaceuticals Inc.24-FEB-11
FinasterideAccord Healthcare Inc.24-MAR-11
FinasterideNorthStar Rx LLC30-MAR-11
FinasterideMylan Institutional Inc.03-JUN-11
FinasterideSun Pharma Global FZE18-AUG-11
FinasterideSun Pharma Global FZE05-OCT-11
FinasterideGreenstone LLC23-NOV-11
FinasterideAmerican Health Packaging17-FEB-12
FinasterideHetero Drugs Limited22-FEB-12
FinasterideActavis Inc.08-APR-12
PropeciaMerck Sharp & Dohme Corp.11-APR-12
PropeciaMerck Sharp & Dohme Corp.11-APR-12
FinasterideDr. Reddy's Laboratories Limited11-MAY-12
FinasterideAurobindo Pharma Limited04-JUN-12
FinasterideIngenus Pharmaceuticals, LLC08-AUG-12
FinasterideDr. Reddy's Laboratories Limited24-AUG-12
FinasterideNorthStar Rx LLC19-SEP-12
Finasteride Bryant Ranch Prepack12-OCT-12
FinasterideDr Reddys Laboratories Inc25-OCT-12
FinasterideCardinal Health16-NOV-12
PropeciaBryant Ranch Prepack17-JAN-13
FinasterideQualitest Pharmaceuticals17-JAN-13
ProscarMerck Sharp & Dohme Corp.18-JAN-13
Finasteride AvKARE, Inc.26-FEB-13
FinasterideLegacy Pharmaceutical Packaging11-MAR-13
FinasterideAurobindo Pharma Limited14-MAR-13
FinasterideTeva Pharmaceuticals USA18-MAR-13
FinasterideCamber Pharmaceuticals, Inc.20-MAR-13
Finasteride AvPAK03-MAY-13

Finasteride Case Reports

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

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About Results

This report contains aggregated drug side effects and adverse events for Finasteride. 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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