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Sutent (Sunitinib) - Adverse Event Reports - Disability - Thrombocytopenia

 



Index of reports > Cases resulting in disability (22) > Cases with Thrombocytopenia (4)

Below is the selection of adverse event reports related to Sutent (Sunitinib) that includes cases resulting in disability where reactions include thrombocytopenia.

Adverse event in female receiving Sutent (Sunitinib)

Reported by a physician from Germany on 2007-10-06

Patient: female, weighing 56.0 kg (123.2 pounds)

Adverse reactions / side effects: Dyspnoea, Flatulence, Palmar-Plantar Erythrodysaesthesia Syndrome, Loss of Consciousness, Mucosal Inflammation, Dysgeusia, Gamma-Glutamyltransferase Increased, Diarrhoea, C-Reactive Protein Increased, Thrombocytopenia, Hypertension, Asthenia, Cardiovascular Disorder, Leukopenia, Epistaxis

Adverse event resulted in: disablity

Suspect drug(s):
Sutent (Sunitinib)

Other drugs received by patient: Beta Blocking Agents; Drug, Unspecified



Adverse event in male receiving Sutent (Sunitinib)

Reported by a physician from Switzerland on 2007-07-05

Patient: male, weighing 92.0 kg (202.4 pounds)

Adverse reactions / side effects: Hepatic Enzyme Abnormal, Abdominal Pain, Cholestasis, Hyperhidrosis, Malaise, Anorexia, Thrombocytopenia, Infection

Adverse event resulted in: disablity

Suspect drug(s):
Sutent (Sunitinib)

Other drugs received by patient: Zestril; Hygroton



Adverse event in 56 year old male receiving Sutent (Sunitinib)

Reported by a individual with unspecified qualification on 2007-04-16

Patient: 56 year old male

Adverse reactions / side effects: Confusional State, Nausea, Therapeutic Agent Toxicity, Somnolence, Anticonvulsant Drug Level Increased, Dizziness, Gait Disturbance, Neutropenia, Thrombocytopenia

Adverse event resulted in: disablity

Suspect drug(s):
Dilantin
    Dosage: 300 mg, unk
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

MS Contin
    Dosage: 20 mg, unk
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Sutent
    Dosage: 50 mg, unk
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication



Adverse event in 56 year old male receiving Sutent (Sunitinib)

Reported by a individual with unspecified qualification on 2007-04-12

Patient: 56 year old male

Adverse reactions / side effects: Confusional State, Nausea, Therapeutic Agent Toxicity, Somnolence, Anticonvulsant Drug Level Increased, Dizziness, Gait Disturbance, Neutropenia, Thrombocytopenia

Adverse event resulted in: disablity

Suspect drug(s):
Dilantin
    Dosage: 300 mg, unk
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

MS Contin
    Dosage: 20 mg, unk
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Sutent
    Dosage: 50 mg, unk
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

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