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Index of reports
> Cases with Condition Aggravated (8)
Below is the selection of side effect reports (a.k.a. adverse event reports) related to Betamethasone (Betamethasone Topical) where reactions include condition aggravated. The selected reports were submitted to the FDA during the sample period of about a year.
Possible Betamethasone side effects in 80 year old male
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2012-06-27
Patient: 80 year old male
Reactions: Pruritus, Hypersensitivity, Drug Ineffective, Drug Interaction, Eczema, Constipation, Rash Pruritic, Psychiatric Symptom, Blood Cholesterol Increased, Rash Pustular, Dermatitis Atopic, Rash Papular, Condition Aggravated, Ulcer, Cerebrovascular Accident, Eosinophilia, Pustular Psoriasis, Mental Impairment, Insomnia, Swelling, Infection
Drug(s) suspected as cause:
Betnovate
Dosage: unk
Indication: Pruritus
Start date: 2007-01-01
Phenergan
Dosage: 1 unk, daily
Indication: Product Used FOR Unknown Indication
Prochlorperazine
Dosage: 3 unk, daily
Indication: Vertigo
Start date: 2007-01-01
Stemetil / 00013301 /
Dosage: unk
Indication: Vertigo
Lipitor
Dosage: unk
Indication: Product Used FOR Unknown Indication
Betamethasone
Dosage: 2 unk, daily
Indication: Product Used FOR Unknown Indication
Start date: 2009-12-30
End date: 2010-03-10
Omeprazole
Dosage: unk
Indication: Product Used FOR Unknown Indication
Bactroban
Dosage: 3 unk, daily
Indication: Skin Ulcer
Start date: 2010-03-10
End date: 2010-03-17
Possible Betamethasone side effects in male
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2012-06-25
Patient: male
Reactions: Hypersensitivity, Pruritus, Drug Ineffective, Drug Interaction, Eczema, Constipation, Rash Pruritic, Psychiatric Symptom, Blood Cholesterol Increased, Dermatitis Atopic, Rash Papular, Condition Aggravated, Cerebrovascular Accident, Ulcer, Eosinophilia, Pustular Psoriasis, Insomnia, Swelling, Infection
Drug(s) suspected as cause:
Prochlorperazine
Indication: Vertigo
Start date: 2007-01-01
Bactroban
Indication: Skin Ulcer
Start date: 2010-03-10
End date: 2010-03-17
Betamethasone
Indication: Product Used FOR Unknown Indication
Start date: 2009-12-30
End date: 2010-03-10
Phenergan
Indication: Product Used FOR Unknown Indication
Lipitor
Indication: Product Used FOR Unknown Indication
Omeprazole
Indication: Product Used FOR Unknown Indication
Betnovate
Indication: Pruritus
Start date: 2007-01-01
Prochlorperazine
Indication: Vertigo
Possible Betamethasone side effects in 80 year old male
Reported by a consumer/non-health professional from United Kingdom on 2012-06-20
Patient: 80 year old male
Reactions: Pruritus, Hypersensitivity, Drug Ineffective, Drug Interaction, Eczema, Constipation, Rash Pruritic, Psychiatric Symptom, Blood Cholesterol Increased, Rash Pustular, Dermatitis Atopic, Rash Papular, Condition Aggravated, Cerebrovascular Accident, Ulcer, Eosinophilia, Mental Impairment, Pustular Psoriasis, Swelling, Insomnia, Infection
Drug(s) suspected as cause:
Prochlorperazine
Indication: Vertigo
Betamethasone
Start date: 2009-12-30
End date: 2010-03-10
Bactroban
Indication: Skin Ulcer
Start date: 2010-03-10
End date: 2010-03-17
Lipitor
Omeprazole
Betnovate
Indication: Pruritus
Start date: 2007-01-01
Other drugs received by patient: Prochlorperazine; Phenergan
Possible Betamethasone side effects in male
Reported by a consumer/non-health professional from United Kingdom on 2012-06-13
Patient: male
Reactions: Pruritus, Hypersensitivity, Drug Ineffective, Drug Interaction, Eczema, Constipation, Rash Pruritic, Psychiatric Symptom, Blood Cholesterol Increased, Rash Pustular, Dermatitis Atopic, Rash Papular, Condition Aggravated, Ulcer, Cerebrovascular Accident, Eosinophilia, Pustular Psoriasis, Mental Impairment, Swelling, Insomnia, Infection
Drug(s) suspected as cause:
Betnovate
Indication: Pruritus
Start date: 2007-01-01
Prochlorperazine
Indication: Vertigo
Lipitor
Indication: Product Used FOR Unknown Indication
Omeprazole
Indication: Product Used FOR Unknown Indication
Bactroban
Indication: Skin Ulcer
Start date: 2010-03-10
End date: 2010-03-17
Betamethasone
Indication: Product Used FOR Unknown Indication
Start date: 2009-12-30
End date: 2010-03-10
Prochlorperazine
Indication: Vertigo
Start date: 2007-01-01
Phenergan
Indication: Product Used FOR Unknown Indication
Possible Betamethasone side effects in 32 year old female
Reported by a health professional (non-physician/pharmacist) from Poland on 2012-06-05
Patient: 32 year old female
Reactions: Caesarean Section, Cardiac Failure, Ventricular Tachycardia, Maternal Exposure During Pregnancy, Condition Aggravated, Atrioventricular Block, Premature Delivery, Atrioventricular Block Second Degree
Drug(s) suspected as cause:
Metoprolol Tartrate
Dosage: 50-75 mg/day
Betamethasone
Furosemide
Dosage: 40 mg
Digitalis
Dosage: 0.1 mg/day
Spironolactone
Dosage: 12.5 mg/day
Isosorbide Mononitrate
Dosage: 20 mg, bid
Dihydralazine
Dosage: 25 mg, tid
Enalapril Maleate
Dosage: 5 mg, bid
Enalapril Maleate
Dosage: 2.5 mg, qd
Possible Betamethasone side effects in 38 year old female
Reported by a physician from Japan on 2012-03-27
Patient: 38 year old female, weighing 52.4 kg (115.3 pounds)
Reactions: Malaise, Cataract, Diarrhoea, Anaemia, Condition Aggravated, Nephritis
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Betamethasone
Dosage: see image
Administration route: Oral
Indication: Lupus Nephritis
Start date: 2008-05-21
End date: 2008-06-04
Betamethasone
Dosage: see image
Administration route: Oral
Indication: Lupus Nephritis
Start date: 2009-05-13
End date: 2009-06-23
Betamethasone
Dosage: see image
Administration route: Oral
Indication: Lupus Nephritis
Start date: 2008-09-04
End date: 2008-10-01
Betamethasone
Dosage: see image
Administration route: Oral
Indication: Lupus Nephritis
Start date: 2009-01-01
End date: 2009-05-12
Betamethasone
Dosage: see image
Administration route: Oral
Indication: Lupus Nephritis
Start date: 2008-07-03
End date: 2008-09-03
Betamethasone
Dosage: see image
Administration route: Oral
Indication: Lupus Nephritis
Start date: 2008-06-05
End date: 2008-07-02
Betamethasone
Dosage: see image
Administration route: Oral
Indication: Lupus Nephritis
Start date: 2009-06-24
End date: 2009-10-06
Betamethasone
Dosage: see image
Administration route: Oral
Indication: Lupus Nephritis
Start date: 2009-10-07
End date: 2010-03-09
Betamethasone
Dosage: see image
Administration route: Oral
Indication: Lupus Nephritis
Start date: 2008-10-02
End date: 2008-12-31
Betamethasone
Dosage: see image
Administration route: Oral
Indication: Lupus Nephritis
Start date: 2010-03-10
End date: 2010-06-01
Tacrolimus
Dosage: 1.5 mg,/d, oral
Administration route: Oral
Indication: Lupus Nephritis
Start date: 2007-10-31
Other drugs received by patient: Ulgut (Benexate Hydrochloride) Capsule; Zantac; Comelian (Dilazep Dihydrochloride); Isodine (Povidone-Iodine) Mouth Wash; Acinon (Nizatidine) Capsule; Slow-FE (Ferrous Sulfate); Onealfa (Alfacalcidol); Prednisolone
Possible Betamethasone side effects in 56 year old male
Reported by a health professional (non-physician/pharmacist) from Poland on 2011-11-25
Patient: 56 year old male
Reactions: Abdominal Pain, Dyspnoea, Nausea, Osteoporosis, Condition Aggravated, Hyponatraemia, Adrenal Insufficiency, Heart Rate Irregular, Pathological Fracture, Blood Pressure Decreased, Acute Myocardial Infarction, Asthenia, Shock
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Betamethasone
Dosage: 2-4 times per week
Indication: Chronic Obstructive Pulmonary Disease
Entocort EC
Dosage: unk unk, unknown
Indication: Chronic Obstructive Pulmonary Disease
Possible Betamethasone side effects in 55 year old female
Reported by a health professional (non-physician/pharmacist) on 2011-10-12
Patient: 55 year old female
Reactions: Hallucination, Auditory, Drug Ineffective, Eczema, Treatment Noncompliance, Rash Pruritic, Weight Increased, Fatigue, Skin Lesion, Sedation, Depression, Eye Pruritus, Drug Hypersensitivity, Condition Aggravated, Eosinophilia, Antipsychotic Drug Level Below Therapeutic, Hyperlipidaemia, Psychotic Disorder, Pigmentation Disorder, Suicide Attempt
Adverse event resulted in: life threatening event, hospitalization
Drug(s) suspected as cause:
Magnesium (Magnesium)
Dosage: 7.5 mg (7.5 mg,1 in 1 d)
Indication: Product Used FOR Unknown Indication
Lorazepam
Dosage: 4 mg (4 mg,1 in 1 d) ; 3 mg (3 mg,1 in 1 d) ; 2 mg (2 mg,1 in 1 d)
Indication: Product Used FOR Unknown Indication
Aripiprazole
Dosage: 60 mg (60 mg,1 in 1 d) ; 45 mg (45 mg,1 in 1 d) ; 30 mg (30 mg,1 in 1 d) ; dose halved (2 d)
Indication: Psychotic Disorder
Pravastatin
Indication: Product Used FOR Unknown Indication
Levothyroxine Sodium
Dosage: 0.05 mg (0.05 mg,1 in 1 d)
Indication: Product Used FOR Unknown Indication
Quetiapine Fumarate
Dosage: 200 mg (200 mg,1 in 1 d)
Indication: Product Used FOR Unknown Indication
Betamethasone
Indication: Product Used FOR Unknown Indication
Lithium Carbonate
Dosage: 625 mg (625 mg,1 in 1 d) ; 900 mg (900 mg,1 in 1 d)
Indication: Product Used FOR Unknown Indication
Sertraline Hydrochloride
Dosage: 100 mg (100 mg,1 in 1 d) ; 150 mg (150 mg,1 in 1 d) ; 200 mg (200 mg,1 in 1 d)
Indication: Depression
Olanzapine
Dosage: 10 mg (10 mg,1 in 1 d)
Indication: Psychotic Disorder
Risperidone
Dosage: 1 mg (1 mg,1 in 1 d)
Indication: Psychotic Disorder
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