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Avodart (Dutasteride) - Reports of Side Effects & Adverse Reactions

 



This is an index of reports of adverse events (side effects, adverse reactions, etc.) related to Avodart (Dutasteride). Click on the relevant link below to view a selection of reports according to the event's seriousness level and/or the nature of the side effect / adverse reaction. Or scroll down to view a sample of recent reports further on this page.

Our database includes reports from Jan 2007 to Dec 2007. The information is not vetted and should not be cosidered as verified clinical evidence.

All cases (144)
     Fatigue (8)Cataract (7)Drug Interaction (7)more >>

Cases resulting in a serious event (140)
     Fatigue (8)Cataract (7)Drug Interaction (7)more >>

Cases resulting in life threatening events (7)
     Blood Pressure Increased (2)Respiratory Disorder (2)Painful Respiration (2)more >>

Cases resulting in hospitalization (27)
     Atrial Fibrillation (4)Loss of Consciousness (4)Abdominal Pain (3)more >>

Cases resulting in disability (9)
     Erectile Dysfunction (3)Fatigue (3)Vomiting (2)more >>

Cases resulting in other serious reactions (108)
     Visual Acuity Reduced (7)Fatigue (7)Jaundice (6)more >>

Below is a sample of reports where side effects / adverse reactions may be related to Avodart (Dutasteride). For a complete list and/or a specific selection of reports, please use the links in the index above.

Adverse event in male receiving Avodart (Dutasteride)

Reported by a consumer/non-health professional from United States on 2007-10-31

Patient: male

Adverse reactions / side effects: Urinary Incontinence, Ill-Defined Disorder

Suspect drug(s):
Avodart (Dutasteride)

Other drugs received by patient: Uroxatral



Adverse event in male receiving Avodart (Dutasteride)

Reported by a consumer/non-health professional from United States on 2007-10-31

Patient: male

Adverse reactions / side effects: Prostatic Specific Antigen Increased, Neoplasm Malignant

Suspect drug(s):
Avodart
    Dosage: .5mg per day
    Administration route: Oral
    Indication: Benign Prostatic Hyperplasia

Hytrin
    Indication: Drug USE FOR Unknown Indication



Adverse event in 68 year old male receiving Avodart (Dutasteride)

Reported by a consumer/non-health professional from United States on 2007-10-31

Patient: 68 year old male

Adverse reactions / side effects: Visual Disturbance, Visual Acuity Reduced, Blindness

Suspect drug(s):
Avodart (Dutasteride)

Other drugs received by patient: Lipitor



Adverse event in 78 year old male receiving Avodart (Dutasteride)

Reported by a consumer/non-health professional from United States on 2007-10-30

Patient: 78 year old male

Adverse reactions / side effects: Mammogram Abnormal, Breast Mass, Gynaecomastia

Suspect drug(s):
Avodart (Dutasteride)

Other drugs received by patient: Flomax



Adverse event in 78 year old male receiving Avodart (Dutasteride)

Reported by a physician from United States on 2007-10-30

Patient: 78 year old male, weighing 90.7 kg (199.6 pounds)

Adverse reactions / side effects: Breast Cancer, Gynaecomastia

Adverse event resulted in: life threatening event

Suspect drug(s):
Avodart (Dutasteride)



Adverse event in male receiving Avodart (Dutasteride)

Reported by a consumer/non-health professional from United States on 2007-10-29

Patient: male

Adverse reactions / side effects: Dysarthria, Dizziness Postural, Head Injury, Middle Ear Effusion, Dizziness, Fall, Sleep Apnoea Syndrome

Suspect drug(s):
Avodart
    Indication: Benign Prostatic Hyperplasia

Flomax
    Administration route: Oral
    Indication: Benign Prostatic Hyperplasia
    Start date: 2006-01-01



Adverse event in male receiving Avodart (Dutasteride)

Reported by a pharmacist from Italy on 2007-10-29

Patient: male

Adverse reactions / side effects: Drug Interaction

Adverse event resulted in: hospitalization

Suspect drug(s):
Avodart (Dutasteride)

Other drugs received by patient: Anticoagulants



Adverse event in 79 year old male receiving Avodart (Dutasteride)

Reported by a consumer/non-health professional from United Kingdom on 2007-10-26

Patient: 79 year old male, weighing 94.0 kg (206.8 pounds)

Adverse reactions / side effects: Chest Pain, Paraesthesia

Suspect drug(s):
Avodart (Dutasteride)

Other drugs received by patient: Bendroflumethiazide; Loperamide HCL; Atenolol; Epilim



Adverse event in 79 year old male receiving Avodart (Dutasteride)

Reported by a consumer/non-health professional from United Kingdom on 2007-10-25

Patient: 79 year old male, weighing 94.0 kg (206.8 pounds)

Adverse reactions / side effects: Chest Pain, Paraesthesia

Suspect drug(s):
Avodart (Dutasteride)

Other drugs received by patient: Bendroflumethiazide; Loperamide HCL; Atenolol; Epilim



Adverse event in 70 year old male receiving Avodart (Dutasteride)

Reported by a consumer/non-health professional from United States on 2007-10-24

Patient: 70 year old male, weighing 75.9 kg (167.0 pounds)

Adverse reactions / side effects: Drug Ineffective, Anaphylactic Reaction, Swollen Tongue

Adverse event resulted in: life threatening event

Suspect drug(s):
Avodart
    Dosage: 1cap per day
    Administration route: Oral
    Indication: Benign Prostatic Hyperplasia

Flomax
    Indication: Drug USE FOR Unknown Indication

Other drugs received by patient: Lisinopril; Amaryl; Toprol-XL; Lopid; Ranitidine HCL



Adverse event in male receiving Avodart (Dutasteride)

Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-24

Patient: male

Adverse reactions / side effects: Pancreatitis

Suspect drug(s):
Avodart
    Indication: Drug USE FOR Unknown Indication

Flomax
    Indication: Drug USE FOR Unknown Indication



Adverse event in male receiving Avodart (Dutasteride)

Reported by a consumer/non-health professional from United States on 2007-10-23

Patient: male

Adverse reactions / side effects: Urinary Incontinence, Feeling Abnormal, Ill-Defined Disorder

Suspect drug(s):
Avodart (Dutasteride)



Adverse event in 58 year old male receiving Avodart (Dutasteride)

Reported by a consumer/non-health professional from United States on 2007-10-22

Patient: 58 year old male

Adverse reactions / side effects: Sperm Count Zero

Suspect drug(s):
Avodart (Dutasteride)

Other drugs received by patient: Flomax



Adverse event in male receiving Avodart (Dutasteride)

Reported by a consumer/non-health professional from United States on 2007-10-22

Patient: male

Adverse reactions / side effects: Prostatic Specific Antigen Increased, Neoplasm Malignant

Suspect drug(s):
Avodart
    Dosage: .5mg per day
    Administration route: Oral
    Indication: Benign Prostatic Hyperplasia

Hytrin
    Indication: Drug USE FOR Unknown Indication



Adverse event in 64 year old male receiving Avodart (Dutasteride)

Reported by a consumer/non-health professional from United States on 2007-10-17

Patient: 64 year old male

Adverse reactions / side effects: Nausea, Illusion, Thermal Burn, Fall, Loss of Consciousness

Suspect drug(s):
Avodart (Dutasteride)

Other drugs received by patient: NO Concurrent Medication



Adverse event in male receiving Avodart (Dutasteride)

Reported by a consumer/non-health professional from United States on 2007-10-17

Patient: male

Adverse reactions / side effects: Breast Cancer Male

Suspect drug(s):
Avodart (Dutasteride)

Other drugs received by patient: Unknown



Adverse event in male receiving Avodart (Dutasteride)

Reported by a consumer/non-health professional from United States on 2007-10-17

Patient: male

Adverse reactions / side effects: Blood Pressure Decreased

Adverse event resulted in: hospitalization

Suspect drug(s):
Avodart (Dutasteride)



Adverse event in male receiving Avodart (Dutasteride)

Reported by a consumer/non-health professional from United States on 2007-10-12

Patient: male

Adverse reactions / side effects: Neoplasm Prostate

Suspect drug(s):
Avodart (Dutasteride)

Other drugs received by patient: Unknown



Adverse event in male receiving Avodart (Dutasteride)

Reported by a consumer/non-health professional from United States on 2007-10-12

Patient: male

Adverse reactions / side effects: Neoplasm Prostate

Suspect drug(s):
Avodart (Dutasteride)

Other drugs received by patient: Unknown



Adverse event in male receiving Avodart (Dutasteride)

Reported by a consumer/non-health professional from United States on 2007-10-11

Patient: male

Adverse reactions / side effects: Infertility

Suspect drug(s):
Avodart (Dutasteride)

Other drugs received by patient: Prilosec; Felden; Acugesic



Adverse event in 87 year old male receiving Avodart (Dutasteride)

Reported by a consumer/non-health professional from United States on 2007-10-11

Patient: 87 year old male

Adverse reactions / side effects: Communication Disorder, Dementia Alzheimer's Type, Dementia

Suspect drug(s):
Avodart (Dutasteride)



Adverse event in 73 year old male receiving Avodart (Dutasteride)

Reported by a consumer/non-health professional from Canada on 2007-10-10

Patient: 73 year old male

Adverse reactions / side effects: Hypoglycaemia

Suspect drug(s):
Avodart (Dutasteride)

Other drugs received by patient: Insulin



Adverse event in 82 year old male receiving Avodart (Dutasteride)

Reported by a consumer/non-health professional from United States on 2007-10-09

Patient: 82 year old male

Adverse reactions / side effects: Haemorrhage

Suspect drug(s):
Avodart (Dutasteride)

Other drugs received by patient: Cipro



Adverse event in 82 year old male receiving Avodart (Dutasteride)

Reported by a consumer/non-health professional from United States on 2007-10-09

Patient: 82 year old male

Adverse reactions / side effects: Haemorrhage

Suspect drug(s):
Avodart (Dutasteride)

Other drugs received by patient: Cipro



Adverse event in male receiving Avodart (Dutasteride)

Reported by a consumer/non-health professional from United States on 2007-10-08

Patient: male

Adverse reactions / side effects: Dysarthria, Dizziness Postural, Head Injury, Middle Ear Effusion, Dizziness, Fall, Sleep Apnoea Syndrome

Suspect drug(s):
Avodart
    Indication: Benign Prostatic Hyperplasia

Flomax
    Administration route: Oral
    Indication: Benign Prostatic Hyperplasia
    Start date: 2006-01-01

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