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Index of reports
> Cases with White Blood Cell Count Decreased (67)
Below is the selection of side effect reports (a.k.a. adverse event reports) related to Copegus (Ribavirin) where reactions include white blood cell count decreased. The selected reports were submitted to the FDA during the sample period of about a year. Reports 1 - 30 of 67 Next >>
Possible Copegus side effects in male
Reported by a consumer/non-health professional from United States on 2012-08-20
Patient: male
Reactions: White Blood Cell Count Decreased, Blood Pressure Decreased, Loss of Consciousness
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Pegasys
Indication: Product Used FOR Unknown Indication
Copegus
Indication: Product Used FOR Unknown Indication
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 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
Reported by a health professional (non-physician/pharmacist) from United States on 2012-08-10
Patient:
Reactions: Weight Decreased, Tinnitus, Chapped Lips, Oropharyngeal Pain, Fatigue, RED Blood Cell Count Decreased, Sinusitis, Back Pain, White Blood Cell Count Decreased, Pneumonia, Dysphagia, Stomatitis, Middle Ear Effusion, Anaemia, Pancytopenia, Rash, LIP Ulceration, Sensory Disturbance, Platelet Count Decreased
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Pegasys
Victrelis
Dosage: 4 df, tid
Copegus
Other drugs received by patient: Ativan; Accolate; Lexapro; Proair (Albuterol Sulfate); Fluticasone Propionate; Procardia XL
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 2012-08-07
Patient: female
Reactions: White Blood Cell Count Decreased, Tongue Discolouration, Hyponatraemia, DRY Skin, Fatigue, Oral Pain, RED Blood Cell Count Decreased, Rash Erythematous, Melanocytic Naevus, Asthenia
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Copegus
Indication: Hepatitis C
Start date: 2011-10-06
Pegasys
Indication: Hepatitis C
Start date: 2011-10-06
Telaprevir
Indication: Hepatitis C
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
Reported by a physician from Japan on 2012-08-01
Patient:
Reactions: White Blood Cell Count Decreased, Malaise, Diarrhoea, Alopecia, Pancytopenia, Pyrexia, Headache, Neutrophil Count Decreased
Drug(s) suspected as cause:
Rebetol
Dosage: 200 mg in the morning and 400 mg in the evening
Administration route: Oral
Indication: Hepatitis C
Start date: 2010-09-16
End date: 2010-12-24
Interferon Beta NOS
Indication: Hepatitis C
Start date: 2010-09-16
End date: 2010-09-21
Copegus
Dosage: 400 mg in the morning and 200 mg in the evening
Administration route: Oral
Indication: Hepatitis C
Start date: 2010-12-27
Interferon Beta NOS
Start date: 2010-10-18
End date: 2010-12-24
Interferon Beta NOS
Start date: 2010-09-24
End date: 2010-10-16
Pegasys
Dosage: 180 qw
Indication: Hepatitis C
Start date: 2010-12-27
Other drugs received by patient: Alfarol; Singulair Tablets 10mg; Advair Diskus 100 / 50; Onealfa
Possible Copegus side effects in female
Reported by a consumer/non-health professional from Brazil on 2012-07-26
Patient: female, weighing 65.0 kg (143.0 pounds)
Reactions: Bone Marrow Disorder, White Blood Cell Count Decreased, Sepsis, Alopecia, Anaemia
Drug(s) suspected as cause:
Pegasys
Indication: Hepatitis C
Copegus
Administration route: Oral
Indication: Hepatitis C
Other drugs received by patient: Acetaminophen
Possible Copegus side effects in female
Reported by a consumer/non-health professional from Canada on 2012-07-18
Patient: female
Reactions: White Blood Cell Count Decreased, RED Blood Cell Count Decreased, Tremor
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Copegus
Dosage: lowered dosage
Administration route: Oral
Copegus
Administration route: Oral
Indication: Hepatitis C
Start date: 2008-05-06
End date: 2008-07-25
Pegasys
Indication: Hepatitis C
Start date: 2008-05-06
End date: 2008-07-25
Possible Copegus side effects in female
Reported by a health professional (non-physician/pharmacist) from United States on 2012-07-09
Patient: female
Reactions: Anxiety, White Blood Cell Count Decreased, RED Blood Cell Count Decreased, Blood Test Abnormal
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Pegasys
Indication: Hepatitis C
Start date: 2012-01-06
Telaprevir
Indication: Product Used FOR Unknown Indication
Pegasys
Boceprevir
Indication: Hepatitis C
Copegus
Indication: Hepatitis C
Start date: 2012-01-06
Possible Copegus side effects in male
Reported by a health professional (non-physician/pharmacist) from United States on 2012-07-03
Patient: male
Reactions: White Blood Cell Count Decreased, RED Blood Cell Count Decreased, Loss of Consciousness
Drug(s) suspected as cause:
Copegus
Dosage: unknown
Indication: Hepatitis C
Start date: 2010-04-01
End date: 2010-06-14
Copegus
Dosage: unknown
Start date: 2011-12-02
Pegasys
Dosage: unknown
Indication: Hepatitis C
Start date: 2010-04-01
End date: 2010-06-14
Pegasys
Dosage: unknown
Start date: 2011-12-02
Other drugs received by patient: Oxycodone HCL
Possible Copegus side effects in female
Reported by a consumer/non-health professional from United States on 2012-07-02
Patient: female
Reactions: White Blood Cell Count Decreased, Tongue Discolouration, Hyponatraemia, DRY Skin, Fatigue, Oral Pain, RED Blood Cell Count Decreased, Melanocytic Naevus, Asthenia
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Pegasys
Indication: Hepatitis C
Start date: 2011-10-06
Copegus
Indication: Hepatitis C
Start date: 2011-10-06
Telaprevir
Indication: Hepatitis C
Possible Copegus side effects in female
Reported by a consumer/non-health professional from United States on 2012-06-26
Patient: female
Reactions: Abdominal Pain, White Blood Cell Count Decreased, Dyspnoea, Chest Discomfort, Haemoglobin Abnormal, Constipation, Abdominal Rigidity, Diarrhoea, Palpitations, RED Blood Cell Count Decreased, Asthenia, Cough, Lethargy
Drug(s) suspected as cause:
Pegasys
Indication: Hepatitis C
Start date: 2012-02-07
Copegus
Copegus
Indication: Hepatitis C
Start date: 2012-02-07
Telaprevir
Indication: Hepatitis C
Start date: 2012-02-07
Possible Copegus side effects in male
Reported by a health professional (non-physician/pharmacist) from United States on 2012-06-26
Patient: male
Reactions: White Blood Cell Count Decreased, Dysphagia, Colon Cancer, Increased Upper Airway Secretion, Drug Ineffective, RED Blood Cell Count Decreased, Oropharyngeal Pain, Cough
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Copegus
Start date: 2011-12-15
End date: 2012-03-09
Copegus
Indication: Hepatitis C
Start date: 1997-01-01
End date: 1997-11-01
Copegus
Start date: 2007-01-01
End date: 2008-01-01
Pegasys
Start date: 2007-01-01
End date: 2008-01-01
Telaprevir
Indication: Hepatitis C
Start date: 2012-01-12
End date: 2012-03-09
Pegasys
Indication: Hepatitis C
Start date: 1997-01-01
End date: 1997-11-01
Pegasys
Start date: 2011-12-15
End date: 2012-03-09
Possible Copegus side effects in male
Reported by a individual with unspecified qualification from Japan on 2012-06-15
Patient: male
Reactions: White Blood Cell Count Decreased, Cellulitis, Muscular Weakness, Hypoaesthesia, Gastritis, Haemoglobin Decreased, Arthralgia, NO Therapeutic Response, Platelet Count Decreased
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Copegus
Administration route: Oral
Indication: Hepatic Cirrhosis
Start date: 2011-10-05
End date: 2011-11-30
Pegasys
Indication: Hepatic Cirrhosis
Start date: 2011-10-05
End date: 2011-11-16
Other drugs received by patient: Urso 250; Magmitt; Amoban; Omeprazole
Possible Copegus side effects in female
Reported by a physician from United States on 2012-06-08
Patient: female
Reactions: Weight Decreased, Tinnitus, Chapped Lips, Oropharyngeal Pain, Fatigue, RED Blood Cell Count Decreased, Sinusitis, White Blood Cell Count Decreased, Back Pain, Pneumonia, Dysphagia, Stomatitis, Middle Ear Effusion, Anaemia, Pancytopenia, Rash, LIP Ulceration, Sensory Disturbance, Platelet Count Decreased
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Pegasys
Indication: Hepatitis C
Start date: 2011-08-29
Copegus
Dosage: divided doses
Indication: Hepatitis C
Start date: 2011-08-29
Boceprevir
Dosage: 4 tablets thrice in day.
Indication: Hepatitis C
Start date: 2011-09-27
Other drugs received by patient: Advair Diskus 100 / 50; Proair HFA; Ativan; Procardia XL; Accolate; Lexapro
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 consumer/non-health professional from United States on 2012-06-01
Patient: male
Reactions: White Blood Cell Count Decreased, Anaemia, Pain
Drug(s) suspected as cause:
Copegus
Administration route: Oral
Indication: Hepatitis C
Start date: 2011-11-14
End date: 2012-02-09
Telaprevir
Indication: Hepatitis C
Start date: 2011-11-14
End date: 2012-02-06
Pegasys
Indication: Hepatitis C
Start date: 2011-11-14
Other drugs received by patient: Neurontin
Possible Copegus side effects in female
Reported by a consumer/non-health professional from United States on 2012-05-28
Patient: female
Reactions: Abdominal Pain, White Blood Cell Count Decreased, Chest Discomfort, Dyspnoea, Haemoglobin Abnormal, Abdominal Rigidity, Palpitations, RED Blood Cell Count Decreased, Asthenia, Cough, Lethargy
Drug(s) suspected as cause:
Pegasys
Indication: Hepatitis C
Start date: 2012-02-07
Copegus
Indication: Hepatitis C
Start date: 2012-02-07
Copegus
Telaprevir
Indication: Hepatitis C
Start date: 2012-02-07
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 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 51 year old male
Reported by a physician from Germany on 2012-05-24
Patient: 51 year old male, weighing 92.0 kg (202.4 pounds)
Reactions: White Blood Cell Count Decreased, Fatigue, Anal Abscess, Skin Disorder, Headache
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Copegus
Dosage: 1000 mg;qd;po 600 mg;qd;po
Administration route: Oral
Indication: Hepatitis C
Start date: 2012-02-16
End date: 2012-04-11
Copegus
Dosage: 1000 mg;qd;po 600 mg;qd;po
Administration route: Oral
Indication: Hepatitis C
Start date: 2012-04-12
Victrelis
Dosage: 2400 mg;qd;po
Administration route: Oral
Indication: Hepatitis C
Start date: 2012-03-15
Pegasys
Dosage: 180 mcg;qw;sc
Indication: Hepatitis C
Start date: 2012-02-16
Possible Copegus side effects in female
Reported by a consumer/non-health professional from United States on 2012-05-23
Patient: female
Reactions: Weight Decreased, Tinnitus, Chapped Lips, Oropharyngeal Pain, Fatigue, RED Blood Cell Count Decreased, Sinusitis, White Blood Cell Count Decreased, Back Pain, Dysphagia, Pneumonia, Stomatitis, Middle Ear Effusion, Anaemia, Pancytopenia, Rash, LIP Ulceration, Sensory Disturbance, Platelet Count Decreased
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Pegasys
Indication: Hepatitis C
Start date: 2011-08-29
Boceprevir
Dosage: 4 tablets thrice in day.
Indication: Hepatitis C
Start date: 2011-09-27
Copegus
Dosage: divided doses
Indication: Hepatitis C
Start date: 2011-08-29
Other drugs received by patient: Procardia XL; Ativan; Accolate; Proair HFA; Advair Diskus 100 / 50; Lexapro
Possible Copegus side effects in male
Reported by a consumer/non-health professional from United States on 2012-05-18
Patient: male
Reactions: Tooth Loss, White Blood Cell Count Decreased
Drug(s) suspected as cause:
Copegus
Indication: Hepatitis C
Start date: 2011-01-01
Pegasys
Indication: Hepatitis C
Start date: 2011-01-01
Possible Copegus side effects in female
Reported by a consumer/non-health professional from United States on 2012-05-15
Patient: female
Reactions: White Blood Cell Count Decreased, Pruritus, Swelling Face, Gingival Bleeding, Mass, DRY Skin, Somnolence, Loss of Consciousness, Faeces Discoloured, Platelet Count Decreased, Dizziness, Asthenia
Drug(s) suspected as cause:
Telaprevir
Dosage: 2 tablets thrice daily
Indication: Hepatitis C
Start date: 2011-12-12
End date: 2012-02-05
Copegus
Dosage: 800 mg divided doses
Administration route: Oral
Indication: Hepatitis C
Start date: 2011-12-12
Pegasys
Copegus
Dosage: in divided doses
Pegasys
Indication: Hepatitis C
Start date: 2011-12-12
Possible Copegus side effects in female
Reported by a consumer/non-health professional from Chile on 2012-05-14
Patient: female, weighing 46.0 kg (101.2 pounds)
Reactions: White Blood Cell Count Decreased, Glossodynia, Hypersensitivity, Goitre, Nausea, Headache, Oropharyngeal Pain, Dermatitis, Tongue Disorder, RED Blood Cell Count Decreased, Ear Pain, Dizziness
Drug(s) suspected as cause:
Copegus
Administration route: Oral
Indication: Hepatitis C
Start date: 2011-06-28
Pegasys
Indication: Hepatitis C
Start date: 2011-06-28
Other drugs received by patient: Clonazepam; Sertraline Hydrochloride
Possible Copegus side effects in male
Reported by a consumer/non-health professional from United States on 2012-05-10
Patient: male, weighing 99.8 kg (219.6 pounds)
Reactions: Weight Decreased, Hypersensitivity, Pruritus, Urticaria, Extrasystoles, Photopsia, Tinea Pedis, Nephrolithiasis, Abdominal Discomfort, Fatigue, Sensation of Foreign Body, Vitreous Floaters, RED Blood Cell Count Decreased, DRY Mouth, White Blood Cell Count Decreased, Viral Infection, Dysphagia, LIP DRY, Tongue DRY, Musculoskeletal Discomfort, Dysgeusia, Dehydration, Vision Blurred, Hypertension, Inflammation
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Pegasys
Indication: Hepatitis C
Copegus
Dosage: divided doses
Administration route: Oral
Indication: Hepatitis C
Other drugs received by patient: Enalapril Maleate; Famotidine
Possible Copegus side effects in female
Reported by a consumer/non-health professional from United States on 2012-05-10
Patient: female
Reactions: White Blood Cell Count Decreased, Abdominal Pain, Chest Discomfort, Dyspnoea, Haemoglobin Abnormal, Abdominal Rigidity, RED Blood Cell Count Decreased, Palpitations, Cough, Lethargy
Drug(s) suspected as cause:
Pegasys
Indication: Hepatitis C
Start date: 2012-02-07
Copegus
Indication: Hepatitis C
Start date: 2012-02-07
Telaprevir
Indication: Hepatitis C
Start date: 2012-02-07
Possible Copegus side effects in female
Reported by a consumer/non-health professional from Chile on 2012-05-10
Patient: female, weighing 53.0 kg (116.6 pounds)
Reactions: White Blood Cell Count Decreased, Hypersensitivity, Glossodynia, Nausea, Goitre, Oropharyngeal Pain, Headache, Tongue Disorder, RED Blood Cell Count Decreased, Dermatitis, Ear Pain, Dizziness
Drug(s) suspected as cause:
Copegus
Administration route: Oral
Indication: Hepatitis C
Start date: 2011-06-28
Pegasys
Indication: Hepatitis C
Start date: 2011-06-28
Other drugs received by patient: Sertraline Hydrochloride; Clonazepam
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