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Copegus (Ribavirin) - Nausea - Suspected Cause - Side Effect Reports

 
 



Index of reports > Cases with Nausea (70)

Below is the selection of side effect reports (a.k.a. adverse event reports) related to Copegus (Ribavirin) where reactions include nausea. The selected reports were submitted to the FDA during the sample period of about a year.

 Reports 1 - 30 of 70   Next >>

Possible Copegus side effects in

Reported by a individual with unspecified qualification from Germany on 2012-08-23

Patient:

Reactions: Renal Failure, Nausea, Haemolysis

Drug(s) suspected as cause:
Copegus



Possible Copegus side effects in female

Reported by a consumer/non-health professional from United States on 2012-08-14

Patient: female

Reactions: Asthma, Weight Increased, Dyspnoea, Fatigue, Dyspnoea Exertional, Nausea, Feeling Abnormal, Decreased Appetite

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Telaprevir
    Indication: Hepatitis C
    Start date: 2012-03-09
    End date: 2012-05-25

Pegasys
    Indication: Hepatitis C
    Start date: 2012-03-09

Copegus
    Dosage: daily divided dose
    Indication: Hepatitis C
    Start date: 2012-03-09

Other drugs received by patient: Fluticasone Propionate; Ventolin



Possible Copegus side effects in male

Reported by a consumer/non-health professional from United States on 2012-08-14

Patient: male

Reactions: Agitation, Weight Decreased, Abdominal Pain, Tinnitus, Pain, Pyrexia, Oropharyngeal Pain, Faeces Discoloured, Anger, Mood Swings, Depression, Tearfulness, Self-Injurious Ideation, White Blood Cell Count Decreased, Vomiting, Type 2 Diabetes Mellitus, Nausea, Cystitis, Costochondritis, Irritability, Emotional Distress, Virologic Failure, Insomnia, Ulcer Haemorrhage

Drug(s) suspected as cause:
Pegasys
    Start date: 2012-02-23

Boceprevir
    Indication: Hepatitis C

Pegasys
    Indication: Hepatitis C
    Start date: 2012-02-20

Copegus
    Indication: Hepatitis C
    Start date: 2012-02-20

Copegus
    Start date: 2012-02-23



Possible Copegus side effects in

Reported by a consumer/non-health professional from United States on 2012-08-10

Patient:

Reactions: Migraine, Vomiting, Nausea, Hyperhidrosis, Diarrhoea, Deafness Unilateral, Anger, Depression, Blindness

Drug(s) suspected as cause:
Pegasys

Victrelis
    Administration route: Oral

Copegus
    Administration route: Oral

Other drugs received by patient: Eprex; Valium



Possible Copegus side effects in

Reported by a health professional (non-physician/pharmacist) from United States on 2012-08-10

Patient:

Reactions: White Blood Cell Count Decreased, Nausea, Rash Papular, Musculoskeletal Pain, Fear, Bone Pain, Flatulence, Abdominal Pain Upper, Rash Pruritic, Dysgeusia, Anxiety, RED Blood Cell Count Decreased, Insomnia, Anger, Depression

Drug(s) suspected as cause:
Copegus
    Dosage: 600 unk, unk
    Administration route: Oral

Victrelis
    Administration route: Oral

Pegasys
    Dosage: 180 unk, unk

Other drugs received by patient: Xanax; Neupogen; Procrit; Lexapro



Possible Copegus side effects in female

Reported by a consumer/non-health professional from United States on 2012-08-10

Patient: female, weighing 48.1 kg (105.9 pounds)

Reactions: Weight Decreased, Vomiting, Nausea, Aphasia, Amnesia, Tremor, Suicidal Ideation, Disturbance in Attention, Depression, Feeling Abnormal

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Copegus
    Administration route: Oral
    Indication: Hepatitis C
    Start date: 2011-07-15
    End date: 2012-04-20

Pegasys
    Indication: Hepatitis C
    Start date: 2011-07-15
    End date: 2012-04-20



Possible Copegus side effects in

Reported by a health professional (non-physician/pharmacist) from United States on 2012-08-10

Patient:

Reactions: Scratch, White Blood Cell Count Decreased, Dyspnoea, Nausea, Drug Ineffective, Drug Hypersensitivity, Hyperhidrosis, Syncope, Middle Insomnia, RED Blood Cell Count Decreased, Injection Site Reaction, Dizziness, Unevaluable Event, Asthenia, Feeling Abnormal

Drug(s) suspected as cause:
Victrelis
    Administration route: Oral

Copegus
    Administration route: Oral

Promethazine

Peginterferon Alfa-2A



Possible Copegus side effects in 42 year old male

Reported by a individual with unspecified qualification from France on 2012-08-09

Patient: 42 year old male

Reactions: Vomiting, Mood Altered, Nausea, Diarrhoea, Underdose, Asthenia

Drug(s) suspected as cause:
Pegasys
    Dosage: 180 microgram, qw
    Indication: Hepatitis C
    Start date: 2011-11-07
    End date: 2012-05-15

Victrelis
    Dosage: 600 mg, tid
    Administration route: Oral
    Indication: Hepatitis C
    Start date: 2011-11-29
    End date: 2011-12-20

Victrelis
    Dosage: 800 mg, tid
    Administration route: Oral
    Start date: 2011-12-21
    End date: 2012-02-20

Copegus
    Dosage: 600 mg, unk
    Administration route: Oral
    Indication: Hepatitis C
    Start date: 2011-11-07
    End date: 2012-05-15

Other drugs received by patient: Abilify; Escitalopram; Atarax



Possible Copegus side effects in male

Reported by a consumer/non-health professional from United States on 2012-08-03

Patient: male

Reactions: Fatigue, Dizziness, Blood Sodium Decreased, Decreased Appetite, Cough, White Blood Cell Count Decreased, Pneumonia, Dyspnoea, Haemoptysis, Nausea, Tuberculosis, Haemoglobin Decreased, Diarrhoea, Arthralgia, Sputum Discoloured, Asthenia, Influenza Like Illness

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Copegus
    Administration route: Oral
    Indication: Hepatitis C
    Start date: 2012-03-16

Pegasys
    Indication: Hepatitis C
    Start date: 2012-03-16

Other drugs received by patient: Lisinopril



Possible Copegus side effects in female

Reported by a consumer/non-health professional from United States on 2012-08-01

Patient: female

Reactions: Abdominal Pain, Thrombosis, Pruritus, Lymphadenopathy, Injection Site Haematoma, Hallucination, Auditory, Tooth Extraction, Headache, Appetite Disorder, Malaise, Menorrhagia, Skin Warm, Muscle Spasms, Blister, Crying, Back Pain, Stomatitis, Rash Erythematous, Insomnia, Swelling, Vision Blurred, Thyroid Disorder, Pain, Constipation, Fatigue, Chest Pain, Bone Disorder, Depression, Hallucination, Decreased Appetite, Blood Pressure Increased, Dyspnoea, Nausea, Musculoskeletal Pain, Rash, Anxiety, Gingival Pain, Psychotic Disorder, Lung Disorder, Oral Pain, Dysuria, Pollakiuria, Memory Impairment, Feeling Abnormal

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Pegasys

Telaprevir
    Indication: Hepatitis C

Ribavirin
    Administration route: Oral
    Indication: Hepatitis C

Pegasys
    Dosage: dosage reported as one injection per week.
    Indication: Hepatitis C
    Start date: 2004-10-30
    End date: 2005-01-09

Copegus
    Administration route: Oral
    Indication: Hepatitis C
    Start date: 2004-10-30
    End date: 2005-01-09

Other drugs received by patient: Wellbutrin; Prozac



Possible Copegus side effects in 54 year old male

Reported by a health professional (non-physician/pharmacist) from United States on 2012-07-24

Patient: 54 year old male, weighing 110.0 kg (242.0 pounds)

Reactions: Vomiting, Nausea, Anaemia, Lactic Acidosis, Ileus, Diarrhoea, Pancreatitis, Systemic Inflammatory Response Syndrome, Leukopenia

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Copegus
    Indication: Hepatitis C
    Start date: 2012-03-01

Telaprevir

Pegasys
    Indication: Hepatitis C
    Start date: 2012-04-10

Telaprevir
    Indication: Hepatitis C
    Start date: 2012-04-10

Other drugs received by patient: Cyclosporine; Myfortic; Tamsulosin HCL; Losartan Potassium; Fluoxetine HCL; Multi-Vitamin; Allopurinol



Possible Copegus side effects in

Reported by a individual with unspecified qualification from France on 2012-07-24

Patient:

Reactions: Vomiting, Nausea, Mood Altered, Diarrhoea, Underdose, Asthenia

Adverse event resulted in: death

Drug(s) suspected as cause:
Victrelis
    Dosage: 800 mg, tid
    Administration route: Oral
    Start date: 2011-12-21
    End date: 2012-02-20

Pegasys
    Dosage: 180 microgram, qw
    Indication: Hepatitis C
    Start date: 2011-11-07
    End date: 2012-05-15

Victrelis
    Dosage: 600 mg, tid
    Administration route: Oral
    Indication: Hepatitis C
    Start date: 2011-11-29
    End date: 2011-12-20

Copegus
    Dosage: 600 mg, unk
    Administration route: Oral
    Indication: Hepatitis C
    Start date: 2011-11-07
    End date: 2012-05-15

Other drugs received by patient: Escitalopram; Abilify; Atarax



Possible Copegus side effects in

Reported by a health professional (non-physician/pharmacist) from France on 2012-07-23

Patient:

Reactions: Fatigue, Dyspnoea Exertional, Rash Generalised, Pruritus, Nausea, Anaemia, Vertigo, Decreased Appetite

Drug(s) suspected as cause:
Norvir
    Dosage: 100 mg, qd
    Indication: HIV Infection
    Start date: 2012-01-03
    End date: 2012-04-23

Isentress
    Dosage: 600 mg, qd
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2012-01-03
    End date: 2012-04-23

Telaprevir
    Dosage: 375 x 6
    Administration route: Oral
    Indication: Hepatitis C
    Start date: 2012-02-12
    End date: 2012-04-25

Reyataz
    Dosage: 300 mg, qd
    Indication: HIV Infection
    Start date: 2012-01-03

Pegasys
    Dosage: 180 a?g, qw
    Indication: Hepatitis C
    Start date: 2012-02-12
    End date: 2012-04-25

Copegus
    Dosage: 1200 mg, qd
    Administration route: Oral
    Indication: Hepatitis C
    Start date: 2012-02-12
    End date: 2012-04-25

Other drugs received by patient: Nexium; Enalapril Maleate and Hydrochlorothiazide; Vitamin D; Gabapentin; Levothyroxine Sodium



Possible Copegus side effects in male

Reported by a physician from France on 2012-07-11

Patient: male, weighing 88.0 kg (193.6 pounds)

Reactions: Nausea, Hepatitis C, Anaemia, Irritability, Dyspnoea Exertional, Fatigue, Vertigo, Proctalgia, Decreased Appetite, Prurigo

Drug(s) suspected as cause:
Copegus
    Administration route: Oral
    Indication: Hepatitis C
    Start date: 2012-02-12
    End date: 2012-04-25

Telaprevir
    Administration route: Oral
    Indication: Hepatitis C
    Start date: 2012-02-12
    End date: 2012-04-25

Isentress
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2012-01-03
    End date: 2012-04-23

Norvir
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2012-01-03
    End date: 2012-04-23

Reyataz
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2012-01-03
    End date: 2012-04-23

Pegasys
    Indication: Hepatitis C
    Start date: 2012-02-12
    End date: 2012-04-25

Other drugs received by patient: Vitamin D; Enalapril Maleate and Hydrochlorothiazide; Levothyroxine Sodium; Nexium; Gabapentin



Possible Copegus side effects in female

Reported by a consumer/non-health professional from United States on 2012-06-26

Patient: female

Reactions: Tinnitus, Vomiting, Nausea, Skin Exfoliation, Scab, Pain, Skin Disorder, Pulmonary Mass, Tremor, Suicidal Ideation, Malaise, Vision Blurred, Disturbance in Attention, Depression, Decreased Appetite

Drug(s) suspected as cause:
Copegus
    Dosage: in divided doses
    Administration route: Oral
    Indication: Hepatitis C

Pegasys
    Indication: Hepatitis C

Copegus
    Dosage: dose decreased



Possible Copegus side effects in female

Reported by a consumer/non-health professional from United States on 2012-06-20

Patient: female, weighing 48.1 kg (105.9 pounds)

Reactions: Weight Decreased, Vomiting, Nausea, Depression, Adverse Reaction, Tremor, Suicidal Ideation

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Pegasys
    Indication: Hepatitis C
    Start date: 2011-07-15
    End date: 2012-04-20

Copegus
    Administration route: Oral
    Indication: Hepatitis C
    Start date: 2011-07-15
    End date: 2012-04-20



Possible Copegus side effects in female

Reported by a physician from Switzerland on 2012-06-15

Patient: female, weighing 78.0 kg (171.6 pounds)

Reactions: Cholelithiasis, Jaundice, Nausea, Psychiatric Decompensation

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Copegus
    Administration route: Oral
    Indication: Hepatitis C
    Start date: 2011-11-07

Copegus
    Dosage: dose reduced
    Start date: 2012-02-27
    End date: 2012-04-22

Pegasys
    Indication: Hepatitis C
    Start date: 2011-11-07
    End date: 2012-04-16

Blinded BI 201335 (Hcv Protease Inhibitor)
    Administration route: Oral
    Start date: 2012-04-23

Blinded BI 201335 (Hcv Protease Inhibitor)
    Administration route: Oral
    Indication: Hepatitis C
    Start date: 2011-11-07
    End date: 2012-01-31

Other drugs received by patient: Exforge; Iberogast; Pantoprazole; Paspertin; Flatulex; Surmontil



Possible Copegus side effects in female

Reported by a physician from United States on 2012-06-14

Patient: female, weighing 72.7 kg (159.9 pounds)

Reactions: Mania, Abdominal Pain, Dyspnoea, Nausea, Urinary Tract Infection, Pancreatic Cyst, Depression

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Escitalopram Oxalate
    Administration route: Oral
    Indication: Depression
    Start date: 2012-04-19
    End date: 2012-04-21

Escitalopram Oxalate
    Administration route: Oral
    Start date: 2012-04-19
    End date: 2012-04-21

Blinded Alisporivir
    Administration route: Oral
    Indication: Hepatitis C
    Start date: 2011-11-10
    End date: 2012-04-17

Escitalopram Oxalate
    End date: 2012-04-23

Pegasys
    Indication: Hepatitis C
    Start date: 2011-11-10
    End date: 2012-04-18

Copegus
    Dosage: 600 mg in every morning and 400 mg in every evening
    Indication: Hepatitis C
    Start date: 2011-11-10
    End date: 2012-04-21



Possible Copegus side effects in male

Reported by a physician from Germany on 2012-06-08

Patient: male, weighing 79.0 kg (173.8 pounds)

Reactions: Pneumonia, Bronchopneumonia, Nausea, Dehydration, General Physical Health Deterioration, Pyrexia, Cystitis, Leukopenia

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Telaprevir
    Administration route: Oral
    Indication: Hepatitis C
    Start date: 2011-12-20
    End date: 2012-03-12

Pegasys
    Indication: Hepatitis C
    Start date: 2011-12-20

Copegus
    Administration route: Oral
    Indication: Hepatitis C
    Start date: 2011-12-20



Possible Copegus side effects in female

Reported by a physician from Switzerland on 2012-06-06

Patient: female, weighing 78.0 kg (171.6 pounds)

Reactions: Jaundice, Blood Bilirubin Increased, Gastritis, Haematocrit Decreased, RED Blood Cell Count Decreased, Depression, Monocyte Percentage Increased, White Blood Cell Count Decreased, Nausea, Alanine Aminotransferase Increased, Haemorrhoids, Psychiatric Decompensation, Haemoglobin Decreased, Cholelithiasis, Anxiety, Blood Potassium Decreased, Aspartate Aminotransferase Increased, Gastroenteritis, Treatment Failure

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Pegasys
    Indication: Hepatitis C
    Start date: 2011-11-07
    End date: 2012-04-16

Copegus
    Administration route: Oral
    Indication: Hepatitis C
    Start date: 2011-11-07

Blinded BI 201335 (Hcv Protease Inhibitor)
    Administration route: Oral
    Indication: Hepatitis C
    Start date: 2011-11-07
    End date: 2012-04-23

Copegus
    Dosage: dose reduced
    End date: 2012-04-22

Other drugs received by patient: Pantoprazole; Surmontil; Iberogast; Paspertin; Flatulex; Exforge; Paspertin



Possible Copegus side effects in male

Reported by a physician from France on 2012-05-30

Patient: male, weighing 88.0 kg (193.6 pounds)

Reactions: Fatigue, Dyspnoea Exertional, Rash Generalised, Pruritus, Nausea, Anaemia, Vertigo, Decreased Appetite

Drug(s) suspected as cause:
Isentress
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2012-01-03
    End date: 2012-04-23

Telaprevir
    Administration route: Oral
    Indication: Hepatitis C
    Start date: 2012-02-09
    End date: 2012-04-23

Peginterferon Alfa-2A
    Indication: Hepatitis C
    Start date: 2012-02-09
    End date: 2012-04-23

Copegus
    Administration route: Oral
    Indication: Hepatitis C
    Start date: 2012-02-09
    End date: 2012-04-23

Reyataz
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2012-01-03
    End date: 2012-04-23

Norvir
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2012-01-03
    End date: 2012-04-23



Possible Copegus side effects in 51 year old male

Reported by a physician from Switzerland on 2012-05-30

Patient: 51 year old male

Reactions: Vomiting, Metabolic Acidosis, Hyperkalaemia, Nausea, Chills, Incorrect Dose Administered, Hyponatraemia, Pyrexia, Renal Failure Chronic, Diarrhoea, Sepsis, Anuria

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Copegus
    Dosage: alternating dose regimen: day 1: 1-0-0 (200 mg/d); day 2: 1-0-1 (400 mg/d)
    Administration route: Oral
    Indication: Hepatitis C
    Start date: 2012-04-13
    End date: 2012-04-23

Pegasys
    Indication: Hepatitis C
    Start date: 2012-04-13
    End date: 2012-04-23

Incivo
    Administration route: Oral
    Indication: Hepatitis C
    Start date: 2012-04-13
    End date: 2012-04-23

Other drugs received by patient: Novorapid; Exforge; Inspra; Pantozol (Switzerland); Euthyrox; Torsemide; Ramipril



Possible Copegus side effects in female

Reported by a consumer/non-health professional from United States on 2012-05-28

Patient: female, weighing 64.0 kg (140.8 pounds)

Reactions: White Blood Cell Count Decreased, Weight Decreased, Pneumonia, Nausea, Anaemia, Haematemesis, Alopecia, Mood Swings, Depression

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Pegasys
    Indication: Hepatitis C
    Start date: 2011-05-18
    End date: 2011-11-17

Copegus
    Indication: Hepatitis C
    Start date: 2011-05-18
    End date: 2011-11-17

Other drugs received by patient: Ondansetron; Wellbutrin; Wellbutrin



Possible Copegus side effects in female

Reported by a individual with unspecified qualification from United Kingdom on 2012-05-28

Patient: female, weighing 58.0 kg (127.6 pounds)

Reactions: Abdominal Pain Lower, Vomiting, Tooth Abscess, Nausea, Dizziness

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Blinded Alisporivir
    Indication: Hepatitis C
    Start date: 2011-11-16

Copegus
    Indication: Hepatitis C
    Start date: 2011-09-26

Codeine Phosphate and Paracetamol
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-01-04

Pegasys
    Indication: Hepatitis C
    Start date: 2011-09-26

Citalopram
    Administration route: Oral
    Indication: Depressed Mood
    Start date: 2011-11-14



Possible Copegus side effects in female

Reported by a consumer/non-health professional from United States on 2012-05-25

Patient: female

Reactions: Abdominal Pain, Megacolon, Weight Decreased, Vomiting, Nausea, Pain, Constipation, Full Blood Count Decreased, Haemoglobin Decreased, Fatigue, Alopecia, Abdominal Distension, Decreased Appetite

Drug(s) suspected as cause:
Copegus
    Dosage: frequency:divided doses, 200 mg in morning, 200 mg in evening
    Administration route: Oral

Pegasys
    Dosage: frequency:per week

Pegasys
    Dosage: frequency:per week
    Indication: Hepatitis C

Copegus
    Dosage: frequency:divided doses, 400 mg in morning, 600 mg in evening
    Administration route: Oral
    Indication: Hepatitis C

Other drugs received by patient: Naprosyn; Seroquel; Milk OF Magnesia TAB; Benadryl; Suboxone; Omeprazole; Guanfacine; Valtrex; Clonazepam; Levoxa; Implanon; Lamictal; Colace



Possible Copegus side effects in female

Reported by a individual with unspecified qualification from United States on 2012-05-25

Patient: female, weighing 72.7 kg (159.9 pounds)

Reactions: Mania, Abdominal Pain, Dyspnoea, Nausea, Urinary Tract Infection, Pancreatic Cyst, Depression

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Escitalopram Oxalate
    Administration route: Oral
    Indication: Depression
    Start date: 2012-04-19
    End date: 2012-04-21

Copegus
    Dosage: 600 mg in every morning and 400 mg in every evening
    Indication: Hepatitis C
    Start date: 2011-11-10
    End date: 2012-04-21

Pegasys
    Indication: Hepatitis C
    Start date: 2011-11-10
    End date: 2012-04-18

Blinded Alisporivir
    Administration route: Oral
    Indication: Hepatitis C
    Start date: 2011-11-10
    End date: 2012-04-17

Escitalopram Oxalate
    End date: 2012-04-23



Possible Copegus side effects in female

Reported by a individual with unspecified qualification from United States on 2012-05-25

Patient: female, weighing 65.4 kg (143.9 pounds)

Reactions: Weight Decreased, Chapped Lips, Skin Burning Sensation, Oedema Peripheral, Nervousness, Anaemia, Hypotonia, Insomnia, Transfusion, Neutropenia, Drug Ineffective, Muscle Tightness, Oral Herpes, Pallor, Fatigue, Haematocrit Decreased, RED Blood Cell Count Decreased, Injection Site Reaction, Dizziness, Candidiasis, Decreased Appetite, White Blood Cell Count Decreased, Vomiting, Nausea, Musculoskeletal Pain, DRY Skin, Diarrhoea, Alopecia, Ammonia Increased, Memory Impairment, Arthritis, Feeling Abnormal, Asthenia

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Pegasys
    Dosage: form: pre-filled syringe; in week 27.180mcg/week
    Indication: Hepatitis C
    Start date: 2010-11-21
    End date: 2011-09-09

Copegus
    Administration route: Oral

Copegus
    Administration route: Oral

Copegus
    Dosage: 600 mg in morning and 400 mg in evening; in week 27
    Administration route: Oral
    Indication: Hepatitis C
    Start date: 2010-11-21
    End date: 2011-09-09

Other drugs received by patient: Hydrocodone Bitartrate; Neurontin; Tramadol HCL; Quinine Sulfate



Possible Copegus side effects in female

Reported by a health professional (non-physician/pharmacist) from Canada on 2012-05-24

Patient: female, weighing 70.0 kg (154.0 pounds)

Reactions: Migraine, Vomiting, Nausea, Hyperhidrosis, Diarrhoea, Deafness Unilateral, Anger, Depression, Blindness

Drug(s) suspected as cause:
Pegasys
    Indication: Hepatitis C
    Start date: 2011-12-14

Copegus
    Administration route: Oral
    Indication: Hepatitis C
    Start date: 2011-12-14

Boceprevir
    Administration route: Oral
    Indication: Hepatitis C

Other drugs received by patient: Valium; Eprex



Possible Copegus side effects in female

Reported by a individual with unspecified qualification from United States on 2012-05-22

Patient: female, weighing 72.7 kg (159.9 pounds)

Reactions: Abdominal Pain, Mania, Dyspnoea, Nausea, Urinary Tract Infection, Pancreatic Cyst, Depression

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Pegasys
    Indication: Hepatitis C
    Start date: 2011-11-10
    End date: 2012-04-18

Copegus
    Dosage: 600 mg in every morning and 400 mg in every evening
    Indication: Hepatitis C
    Start date: 2011-11-10
    End date: 2012-04-21

Escitalopram Oxalate
    End date: 2012-04-23

Blinded Alisporivir
    Administration route: Oral
    Indication: Hepatitis C
    Start date: 2011-11-10
    End date: 2012-04-17

Escitalopram Oxalate
    Administration route: Oral
    Indication: Depression
    Start date: 2012-04-19
    End date: 2012-04-21



Possible Copegus side effects in male

Reported by a physician from Germany on 2012-05-18

Patient: male, weighing 80.0 kg (176.0 pounds)

Reactions: Vomiting, Concussion, Head Injury, Angina Pectoris, Nausea, Altered State of Consciousness

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Pegasys
    Indication: Hepatitis C
    Start date: 2011-05-20

Copegus
    Administration route: Oral
    Indication: Hepatitis C
    Start date: 2011-05-20



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