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This is an index of reports of adverse events (side effects, adverse reactions, etc.) related to Nexavar (Sorafenib). 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 (519)
Cases resulting in a serious event (433)
Cases resulting in death (99)
Cases resulting in life threatening events (24)
Cases resulting in hospitalization (170)
Cases resulting in disability (37)
Cases resulting in other serious reactions (235)
Below is a sample of reports where side effects / adverse reactions may be related to Nexavar (Sorafenib). For a complete list and/or a specific selection of reports, please use the links in the index above.
Adverse event in male receiving Nexavar (Sorafenib)
Reported by a individual with unspecified qualification from United States on 2007-10-31
Patient: male
Adverse reactions / side effects: Blood Pressure Increased, Diarrhoea
Suspect drug(s):
Nexavar (Sorafenib)
Adverse event in 70 year old female receiving Nexavar (Sorafenib)
Reported by a individual with unspecified qualification from United States on 2007-10-31
Patient: 70 year old female, weighing 61.7 kg (135.7 pounds)
Adverse reactions / side effects: Pain in Extremity, Skin Exfoliation, Palmar-Plantar Erythrodysaesthesia Syndrome, Rash, Paraesthesia, Dysphonia, Diarrhoea, Sensory Disturbance, Blister
Suspect drug(s):
Nexavar
Dosage: see image
Administration route: Oral
Indication: Renal Cell Carcinoma Stage Unspecified
Start date: 2006-01-10
End date: 2006-01-23
Nexavar
Dosage: see image
Administration route: Oral
Indication: Renal Cell Carcinoma Stage Unspecified
Start date: 2006-06-06
End date: 2007-08-10
Nexavar
Dosage: see image
Administration route: Oral
Indication: Renal Cell Carcinoma Stage Unspecified
Start date: 2006-01-30
Nexavar
Dosage: see image
Administration route: Oral
Indication: Renal Cell Carcinoma Stage Unspecified
Start date: 2007-08-18
Other drugs received by patient: Lotrel; Lipitor; Bumex; Atenolol
Adverse event in female receiving Nexavar (Sorafenib)
Reported by a consumer/non-health professional from United States on 2007-10-31
Patient: female
Adverse reactions / side effects: Stomach Discomfort
Suspect drug(s):
Nexavar (Sorafenib)
Adverse event in male receiving Nexavar (Sorafenib)
Reported by a individual with unspecified qualification from United States on 2007-10-31
Patient: male
Adverse reactions / side effects: Pain in Extremity, Palmar-Plantar Erythrodysaesthesia Syndrome, Nasal Congestion, Constipation, Throat Tightness, Diarrhoea, Mouth Breathing, Pharyngolaryngeal Pain, Gait Disturbance, Ear Congestion, Blister
Suspect drug(s):
Nexavar
Dosage: 400 mg, bid, oral; 600 mg, total daily, oral
Administration route: Oral
Indication: Hepatic Neoplasm Malignant
Start date: 2007-03-01
Nexavar
Dosage: 400 mg, bid, oral; 600 mg, total daily, oral
Administration route: Oral
Indication: Metastases TO Abdominal Cavity
Start date: 2007-03-01
Other drugs received by patient: Aspirin
Adverse event in receiving Nexavar (Sorafenib)
Reported by a physician from United States on 2007-10-31
Patient:
Adverse reactions / side effects: Diarrhoea
Suspect drug(s):
Nexavar (Sorafenib)
Adverse event in receiving Nexavar (Sorafenib)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-31
Patient:
Adverse reactions / side effects: Urticaria, Rash, Rash Maculo-Papular
Suspect drug(s):
Nexavar (Sorafenib)
Adverse event in 86 year old female receiving Nexavar (Sorafenib)
Reported by a individual with unspecified qualification from United States on 2007-10-31
Patient: 86 year old female
Adverse reactions / side effects: Pruritus, Alopecia, Rash Macular, Paraesthesia
Suspect drug(s):
Nexavar (Sorafenib)
Other drugs received by patient: Lisinopril; Mucinex; Benadryl
Adverse event in 56 year old male receiving Nexavar (Sorafenib)
Reported by a individual with unspecified qualification from United States on 2007-10-31
Patient: 56 year old male
Adverse reactions / side effects: Blood Pressure Increased, Pruritus, Swelling Face, Pain in Extremity, Skin Exfoliation, Rash, Erythema, Paraesthesia, Burning Sensation
Suspect drug(s):
Nexavar
Dosage: 40 mg bid oral ; 400 mg om oral
Administration route: Oral
Indication: Renal Cell Carcinoma Stage Unspecified
Start date: 2007-05-03
End date: 2007-05-01
Nexavar
Dosage: 40 mg bid oral ; 400 mg om oral
Administration route: Oral
Indication: Renal Cell Carcinoma Stage Unspecified
Start date: 2007-05-20
Other drugs received by patient: Amlodipine; Lunesta; Acetaminophen
Adverse event in 53 year old male receiving Nexavar (Sorafenib)
Reported by a individual with unspecified qualification from United States on 2007-10-31
Patient: 53 year old male
Adverse reactions / side effects: Drug Toxicity, Burning Sensation, Localised Infection, Fatigue, Oedema Peripheral, Pyrexia, Rash, Erythema
Adverse event resulted in: hospitalization
Suspect drug(s):
Nexavar
Dosage: 400 mg, bid, oral
Administration route: Oral
Indication: Metastases TO Bone
Start date: 2006-07-12
End date: 2006-10-01
Nexavar
Dosage: 400 mg, bid, oral
Administration route: Oral
Indication: Renal Cell Carcinoma Stage Unspecified
Start date: 2006-07-12
End date: 2006-10-01
Other drugs received by patient: Percocet; Zetia; Celebrex; Testosterone; Oscal (Calcium Carbonate)
Adverse event in male receiving Nexavar (Sorafenib)
Reported by a individual with unspecified qualification from United States on 2007-10-31
Patient: male
Adverse reactions / side effects: Rash
Suspect drug(s):
Nexavar (Sorafenib)
Adverse event in male receiving Nexavar (Sorafenib)
Reported by a individual with unspecified qualification from United States on 2007-10-31
Patient: male
Adverse reactions / side effects: Palmar-Plantar Erythrodysaesthesia Syndrome
Suspect drug(s):
Nexavar (Sorafenib)
Adverse event in male receiving Nexavar (Sorafenib)
Reported by a physician from United States on 2007-10-31
Patient: male
Adverse reactions / side effects: Lower Gastrointestinal Haemorrhage
Suspect drug(s):
Nexavar (Sorafenib)
Adverse event in 61 year old female receiving Nexavar (Sorafenib)
Reported by a individual with unspecified qualification from United States on 2007-10-31
Patient: 61 year old female
Adverse reactions / side effects: Pain in Extremity, Diarrhoea, Oral Pain
Suspect drug(s):
Nexavar (Sorafenib)
Adverse event in 58 year old female receiving Nexavar (Sorafenib)
Reported by a individual with unspecified qualification from United States on 2007-10-31
Patient: 58 year old female, weighing 74.8 kg (164.7 pounds)
Adverse reactions / side effects: Stomatitis, Abdominal Abscess, Diarrhoea, Pneumoperitoneum, Rash, Diverticular Perforation
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Nexavar
Dosage: 400 mg, bid, oral, 200 mg, bid, oral
Administration route: Oral
Indication: Renal Cell Carcinoma Stage Unspecified
Start date: 2006-11-01
End date: 2007-01-01
Nexavar
Dosage: 400 mg, bid, oral, 200 mg, bid, oral
Administration route: Oral
Indication: Renal Cell Carcinoma Stage Unspecified
Start date: 2007-01-01
End date: 2007-07-06
Other drugs received by patient: Glipizide; Avandia; Klor-CON; Mavik; Allopurinol; Zyrtec; Dolobid; Lasix; Vytorin; Centrum Silver; Toprol-XL; Imodium
Adverse event in 82 year old male receiving Nexavar (Sorafenib)
Reported by a consumer/non-health professional from United States on 2007-10-31
Patient: 82 year old male
Adverse reactions / side effects: Nausea, Rash Pruritic
Suspect drug(s):
Nexavar
Dosage: 400 mg, bid, oral
Administration route: Oral
Indication: Lung Neoplasm Malignant
Start date: 2007-07-21
Nexavar
Dosage: 400 mg, bid, oral
Administration route: Oral
Indication: Renal Cell Carcinoma Stage Unspecified
Start date: 2007-07-21
Adverse event in female receiving Nexavar (Sorafenib)
Reported by a individual with unspecified qualification from United States on 2007-10-31
Patient: female
Adverse reactions / side effects: Diarrhoea
Suspect drug(s):
Nexavar (Sorafenib)
Adverse event in male receiving Nexavar (Sorafenib)
Reported by a individual with unspecified qualification from United States on 2007-10-31
Patient: male
Adverse reactions / side effects: Diarrhoea
Suspect drug(s):
Nexavar (Sorafenib)
Adverse event in receiving Nexavar (Sorafenib)
Reported by a physician from United States on 2007-10-31
Patient:
Adverse reactions / side effects: Blood Pressure Increased, Anaemia
Suspect drug(s):
Nexavar (Sorafenib)
Adverse event in 62 year old female receiving Nexavar (Sorafenib)
Reported by a individual with unspecified qualification from United States on 2007-10-31
Patient: 62 year old female, weighing 78.9 kg (173.6 pounds)
Adverse reactions / side effects: Weight Decreased, Arthralgia, Diarrhoea
Suspect drug(s):
Nexavar (Sorafenib)
Adverse event in male receiving Nexavar (Sorafenib)
Reported by a individual with unspecified qualification from United States on 2007-10-31
Patient: male
Adverse reactions / side effects: Visual Disturbance
Suspect drug(s):
Nexavar (Sorafenib)
Adverse event in 76 year old male receiving Nexavar (Sorafenib)
Reported by a individual with unspecified qualification from United States on 2007-10-31
Patient: 76 year old male
Adverse reactions / side effects: Diarrhoea, Rash
Suspect drug(s):
Nexavar (Sorafenib)
Adverse event in 62 year old male receiving Nexavar (Sorafenib)
Reported by a individual with unspecified qualification from United States on 2007-10-31
Patient: 62 year old male
Adverse reactions / side effects: Squamous Cell Carcinoma, Skin Lesion
Suspect drug(s):
Nexavar
Dosage: 200 mg, qd, oral
Administration route: Oral
Indication: Metastases TO Kidney
Start date: 2007-01-01
Nexavar
Dosage: 200 mg, qd, oral
Administration route: Oral
Indication: Metastatic Renal Cell Carcinoma
Start date: 2007-01-01
Adverse event in receiving Nexavar (Sorafenib)
Reported by a physician from United States on 2007-10-31
Patient:
Adverse reactions / side effects: Palmar-Plantar Erythrodysaesthesia Syndrome, Rash
Suspect drug(s):
Nexavar (Sorafenib)
Adverse event in receiving Nexavar (Sorafenib)
Reported by a physician from United States on 2007-10-31
Patient:
Adverse reactions / side effects: Palmar-Plantar Erythrodysaesthesia Syndrome
Suspect drug(s):
Nexavar (Sorafenib)
Adverse event in 77 year old male receiving Nexavar (Sorafenib)
Reported by a physician from United States on 2007-10-31
Patient: 77 year old male
Adverse reactions / side effects: Hypogeusia, Diarrhoea, Headache
Suspect drug(s):
Nexavar
Dosage: 400 mg, bid, oral
Administration route: Oral
Indication: Metastases TO Lung
Start date: 2006-04-20
End date: 2006-05-01
Nexavar
Dosage: 400 mg, bid, oral
Administration route: Oral
Indication: Renal Cell Carcinoma Stage Unspecified
Start date: 2006-04-20
End date: 2006-05-01
Nexavar
Dosage: 400 mg, bid, oral
Administration route: Oral
Indication: Metastases TO Lung
Start date: 2006-05-22
End date: 2006-05-23
Nexavar
Dosage: 400 mg, bid, oral
Administration route: Oral
Indication: Renal Cell Carcinoma Stage Unspecified
Start date: 2006-05-22
End date: 2006-05-23
Nexavar
Dosage: 400 mg, bid, oral
Administration route: Oral
Indication: Metastases TO Lung
Start date: 2006-05-24
Nexavar
Dosage: 400 mg, bid, oral
Administration route: Oral
Indication: Renal Cell Carcinoma Stage Unspecified
Start date: 2006-05-24
Other drugs received by patient: Lipitor; Bisoprolol Fumarate and Hydrochlorothiazide; Calcium; MVI (Vitamins Nos); Vicodin; Imdur; Fish OIL; Prilosec; Oxycodone HCL; Senna; Colace
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