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CLOBETASOL PROPIONATE

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Clobetasol Propionate Adverse Events Reported to the FDA Over Time

How are Clobetasol Propionate adverse event reports trending over time?

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

Most Common Clobetasol Propionate Adverse Events Reported to the FDA

What are the most common Clobetasol Propionate adverse events reported to the FDA?

Drug Ineffective
69 (3.28%)
Incorrect Drug Administration Durat...
47 (2.24%)
Product Quality Issue
42 (2%)
Off Label Use
38 (1.81%)
Headache
27 (1.28%)
Burning Sensation
24 (1.14%)
Erythema
24 (1.14%)
Pruritus
24 (1.14%)
Condition Aggravated
22 (1.05%)
Skin Atrophy
22 (1.05%)
Blood Cortisol Decreased
21 (1%)
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Cushingoid
20 (.95%)
Necrotising Fasciitis
18 (.86%)
Overdose
16 (.76%)
Rash
16 (.76%)
Application Site Pain
15 (.71%)
Drug Administration Error
15 (.71%)
Vomiting
15 (.71%)
Weight Increased
15 (.71%)
Adrenal Insufficiency
14 (.67%)
Hypertension
14 (.67%)
Alopecia
13 (.62%)
Dyspnoea
13 (.62%)
Oedema Peripheral
13 (.62%)
Psoriasis
13 (.62%)
Blister
12 (.57%)
Cellulitis
12 (.57%)
Hypersensitivity
12 (.57%)
Squamous Cell Carcinoma
12 (.57%)
Diabetes Mellitus
11 (.52%)
Glaucoma
11 (.52%)
Growth Retardation
11 (.52%)
Inappropriate Schedule Of Drug Admi...
11 (.52%)
Pain
11 (.52%)
Skin Discolouration
11 (.52%)
Adrenal Suppression
10 (.48%)
Asthenia
10 (.48%)
Drug Exposure During Pregnancy
10 (.48%)
Dry Skin
10 (.48%)
Hair Disorder
10 (.48%)
Malaise
10 (.48%)
Medication Error
10 (.48%)
Accidental Exposure
9 (.43%)
Dizziness
9 (.43%)
Drug Dispensing Error
9 (.43%)
Hypotension
9 (.43%)
Pain In Extremity
9 (.43%)
Skin Disorder
9 (.43%)
Cataract
8 (.38%)
Drug Dependence
8 (.38%)
Ecchymosis
8 (.38%)
Obesity
8 (.38%)
Pyrexia
8 (.38%)
Telangiectasia
8 (.38%)
Application Site Erythema
7 (.33%)
Chest Pain
7 (.33%)
Convulsion
7 (.33%)
Drug Eruption
7 (.33%)
Dysgeusia
7 (.33%)
Lymphopenia
7 (.33%)
Skin Striae
7 (.33%)
Swelling Face
7 (.33%)
Abortion Induced
6 (.29%)
Application Site Pruritus
6 (.29%)
Blepharitis
6 (.29%)
Blood Corticotrophin Decreased
6 (.29%)
Blood Pressure Increased
6 (.29%)
Cerebrovascular Accident
6 (.29%)
Decreased Appetite
6 (.29%)
Dermatitis
6 (.29%)
Diarrhoea
6 (.29%)
Expired Drug Administered
6 (.29%)
Haemoglobin Decreased
6 (.29%)
Increased Appetite
6 (.29%)
Muscle Twitching
6 (.29%)
Muscular Weakness
6 (.29%)
Neck Pain
6 (.29%)
Peptic Ulcer Perforation
6 (.29%)
Peritonitis
6 (.29%)
Platelet Count Increased
6 (.29%)
Pregnancy
6 (.29%)
Scar
6 (.29%)
Skin Exfoliation
6 (.29%)
Skin Infection
6 (.29%)
Skin Irritation
6 (.29%)
Wound Dehiscence
6 (.29%)
Atrophy
5 (.24%)
Blood Glucose Increased
5 (.24%)
Caustic Injury
5 (.24%)
Chorioretinopathy
5 (.24%)
Death
5 (.24%)
Drug Administered At Inappropriate ...
5 (.24%)
Erysipelas
5 (.24%)
Fall
5 (.24%)
Gangrene
5 (.24%)
Hair Colour Changes
5 (.24%)
Hepatic Enzyme Increased
5 (.24%)
Hypercholesterolaemia
5 (.24%)
Hypertrichosis
5 (.24%)
Ill-defined Disorder
5 (.24%)
Incorrect Dose Administered
5 (.24%)

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

What are the most common Clobetasol Propionate adverse events reported to the FDA?

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

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

Psoriasis
400
Product Used For Unknown Indication
141
Eczema
77
Rash
72
Drug Use For Unknown Indication
60
Dermatitis Diaper
36
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Pruritus
33
Pemphigoid
29
Lichen Sclerosus
29
Psoriatic Arthropathy
20
Dermatitis
17
Skin Disorder
16
Dermatitis Atopic
15
Pustular Psoriasis
14
Alopecia
11
Erythema
10
Dermatosis
10
Skin Irritation
10
Dry Skin
10
Skin Lesion
9
Cellulitis
8
Skin Cosmetic Procedure
8
Folliculitis
7
Palmar-plantar Erythrodysaesthesia ...
7
Seborrhoeic Dermatitis
7
Graft Versus Host Disease
7
Vitiligo
6
Cutaneous Lupus Erythematosus
6
Pyoderma Gangrenosum
6
Rash Maculo-papular
5
Lichen Planus
5
Dermatitis Contact
5
Vulvovaginitis
5
Alopecia Areata
5
Wound
4
Hyperkeratosis Palmaris And Plantar...
4
Acrodermatitis
4
Drug Eruption
4
Rash Papular
4
Paronychia
4
Herpes Virus Infection
3
Systemic Lupus Erythematosus
3
Skin Reaction
3
Dermatitis Acneiform
3
Erythema Multiforme
3
Swelling
3
Atrophic Vulvovaginitis
3
Dermatitis Exfoliative
3
Skin Plaque
2
Skin Discolouration
2
Arthropod Bite
2

Drug Labels

LabelLabelerEffective
Clobexshampoo 0.05%DPT Laboratories, Ltd.17-AUG-09
Clobetasol PropionateDPT Laboratories, Ltd.14-OCT-09
Clobetasol PropionateHi-Tech Pharmacal Co., Inc.04-JUN-10
Clobetasol PropionateHi-Tech Pharmacal Co., Inc.04-JUN-10
Clobetasol PropionatePhysicians Total Care, Inc.04-JUN-10
Clobetasol PropionatePhysicians Total Care, Inc.04-JUN-10
Clobetasol PropionateRebel Distributors Corp23-SEP-10
Clobetasol PropionateGolden State Medical Supply, Inc.10-NOV-10
Clobetasol PropionateGolden State Medical Supply, Inc.10-NOV-10
Clobetasol PropionateRebel Distributors Corp01-DEC-10
Clobetasol PropionatePhysicians Total Care, Inc.28-DEC-10
Clobetasol PropionatePerrigo New York Inc22-MAR-11
OluxStiefel Laboratories Inc29-JUN-11
Clobetasol PropionatePrasco Laboratories19-JUL-11
Clobetasol PropionatePhysicians Total Care, Inc.19-JUL-11
Clobetasol PropionateTaro Pharmaceuticals U.S.A., Inc.20-SEP-11
Clobetasol PropionateTaro Pharmaceuticals U.S.A., Inc.29-SEP-11
Clobetasol PropionatePerrigo New York Inc11-NOV-11
Clobetasol PropionateHi-Tech Pharmacal Co., Inc.22-NOV-11
Clobetasol PropionatePreferred Pharmaceuticals, Inc30-JAN-12
Clobetasol PropionateMorton Grove Pharmaceuticals, Inc.30-JAN-12
Clobetasol PropionateE. FOUGERA & CO. A division of Fougera Pharmaceuticals Inc.27-FEB-12
Clobetasol PropionateRebel Distributors Corp06-MAR-12
Clobetasol PropionatePhysicians Total Care, Inc.02-APR-12
TemovatePharmaDerm, A division of Fougera Pharmaceuticals Inc.15-APR-12
TemovatePharmaDerm A division of Fougera Pharmaceuticals Inc.15-APR-12
Clobetasol PropionatePreferred Pharmaceuticals, Inc23-APR-12
Clobetasol PropionatePreferred Pharmaceuticals, Inc23-APR-12
OluxPhysicians Total Care, Inc.02-MAY-12
Clobetasol PropionateUnit Dose Services07-JUN-12
Clobetasol PropionateE. FOUGERA & CO., A division of Fougera Pharmaceuticals Inc.07-JUN-12
Clobetasol PropionateE. FOUGERA & CO. A division of Fougera Pharmaceuticals Inc.12-JUN-12
Clobetasol PropionateTaro Pharmaceuticals U.S.A., Inc.14-JUN-12
Clobetasol Propionate EmulsionPrasco Laboratories20-JUN-12
CormaxECR Pharmaceuticals Co., Inc.25-JUN-12
TemovatePharmaDerm a division of Fougera Pharmaceuticals Inc.03-JUL-12
TemovatePharmaDerm, A division of Fougera Pharmaceuticals Inc.05-JUL-12
Temovate Scalp Application PharmaDerm, A division of Fougera Pharmaceuticals Inc.06-JUL-12
Clobetasol PropionateTaro Pharmaceuticals U.S.A., Inc.16-JUL-12
Clobetasol PropionateHi-Tech Pharmacal Co., Inc.22-AUG-12
Clobex Galderma Laboratories, L.P.01-SEP-12
Olux-eStiefel Laboratories Inc10-SEP-12
Clobetasol PropionatePerrigo New York Inc26-SEP-12
ClobexGalderma Laboratories, L.P.01-NOV-12
Clobetasol PropionatePaddock Laboratories, LLC.01-NOV-12
Temovate EPharmaDerm a division of Fougera Pharmaceuticals Inc.03-DEC-12
ClobexGalderma Laboratories, L.P.30-JAN-13
Clobetasol PropionateSandoz Inc.30-JAN-13
Clobetasol Propionateemollient FormulationPerrigo New York Inc04-FEB-13
Clobetasol PropionateActavis Mid Atlantic LLC22-FEB-13
Clobetasol PropionateActavis Mid Atlantic LLC08-MAR-13
Clobetasol PropionatePreferred Pharmaceuticals, Inc.19-APR-13
Clobetasol PropionatePreferred Pharmaceuticals, Inc19-APR-13
Olux-eStiefel Laboratories Inc24-APR-13

Clobetasol Propionate Case Reports

What Clobetasol Propionate 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 Clobetasol Propionate. 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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