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Sutent (Sunitinib) - Reports of Side Effects & Adverse Reactions

 



This is an index of reports of adverse events (side effects, adverse reactions, etc.) related to Sutent (Sunitinib). 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 (950)
     Death (136)Thrombocytopenia (76)Fatigue (59)more >>

Cases resulting in a serious event (940)
     Death (136)Thrombocytopenia (75)Fatigue (58)more >>

Cases resulting in death (287)
     Disease Progression (41)Thrombocytopenia (21)Dyspnoea (17)more >>

Cases resulting in life threatening events (37)
     Vomiting (5)Sepsis (5)Neutropenia (5)more >>

Cases resulting in hospitalization (387)
     Thrombocytopenia (47)Vomiting (35)Nausea (29)more >>

Cases resulting in disability (22)
     Nausea (6)Fatigue (4)Thrombocytopenia (4)more >>

Cases resulting in other serious reactions (483)
     Fatigue (49)Hypertension (41)Diarrhoea (39)more >>

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

Adverse event in male receiving Sutent (Sunitinib)

Reported by a physician from Iceland on 2007-10-31

Patient: male, weighing 55.0 kg (121.0 pounds)

Adverse reactions / side effects: Pneumonia, Bronchial Fistula, Bronchitis, Hypertension

Adverse event resulted in: death, hospitalization

Suspect drug(s):
Sutent
    Administration route: Oral
    Indication: Renal Cell Carcinoma Stage Unspecified
    Start date: 2006-10-27
    End date: 2007-05-25

Sutent

Other drugs received by patient: Valsartan



Adverse event in female receiving Sutent (Sunitinib)

Reported by a individual with unspecified qualification from Argentina on 2007-10-31

Patient: female, weighing 73.0 kg (160.6 pounds)

Adverse reactions / side effects: White Blood Cell Count Decreased, Blood Pressure Increased, RED Blood Cell Count Decreased, Platelet Count Decreased, Liver Disorder

Suspect drug(s):
Sutent (Sunitinib)

Other drugs received by patient: Enalapril Maleate; Clonazepam; Metformin HCL



Adverse event in male receiving Sutent (Sunitinib)

Reported by a physician on 2007-10-31

Patient: male, weighing 109.0 kg (239.8 pounds)

Adverse reactions / side effects: Myelitis Transverse

Adverse event resulted in: hospitalization

Suspect drug(s):
Sutent (Sunitinib)

Other drugs received by patient: Phenytoin; Keppra; Lamotrigine; Neurontin; Atenolol; Bethanechol; Tamsulosin HCL; Lovenox; Psyllium; Nexium; Oxycodone HCL; Oxycontin; Zoloft



Adverse event in female receiving Sutent (Sunitinib)

Reported by a individual with unspecified qualification from United Kingdom on 2007-10-31

Patient: female, weighing 77.0 kg (169.4 pounds)

Adverse reactions / side effects: Neutropenic Sepsis

Adverse event resulted in: hospitalization

Suspect drug(s):
Docetaxel
    Dosage: daily dose:140mg-freq:cyclic every 3 weeks
    Indication: Breast Cancer Metastatic

Sutent
    Dosage: daily dose:37.5mg-freq:cyclic
    Administration route: Oral
    Indication: Breast Cancer Metastatic

Other drugs received by patient: Movicol; Ezetrol; Metoclopramide; Dexamethasone 0.5mg TAB



Adverse event in male receiving Sutent (Sunitinib)

Reported by a physician from France on 2007-10-31

Patient: male

Adverse reactions / side effects: Fatigue, Skin Hypertrophy

Adverse event resulted in: disablity

Suspect drug(s):
Sutent (Sunitinib)



Adverse event in female receiving Sutent (Sunitinib)

Reported by a individual with unspecified qualification from United States on 2007-10-31

Patient: female, weighing 70.8 kg (155.8 pounds)

Adverse reactions / side effects: Gastroenteritis Proteus, Skin Graft, Pseudomonas Infection, Hyperplasia, Staphylococcal Infection, Skin Odour Abnormal, Skin Infection, Vasculitis, Culture Wound Positive, Infected Skin Ulcer

Adverse event resulted in: hospitalization

Suspect drug(s):
Paclitaxel
    Indication: Breast Cancer Metastatic
    Start date: 2006-03-30
    End date: 2006-09-07

Sutent
    Administration route: Oral
    Indication: Breast Cancer Metastatic
    Start date: 2006-03-30
    End date: 2007-10-23

Other drugs received by patient: Loperamide HCL; Epoetin Alfa; Neupogen; Ultram; Esomeprazole Magnesium; Fexofenadine; Furosemide; Potassium Chloride; Magnesium Sulfate



Adverse event in 66 year old female receiving Sutent (Sunitinib)

Reported by a physician from Greece on 2007-10-31

Patient: 66 year old female

Adverse reactions / side effects: Hepatitis

Suspect drug(s):
Sutent (Sunitinib)

Other drugs received by patient: Hydroxocobalamin Acetate; Fero-Folic



Adverse event in 36 year old male receiving Sutent (Sunitinib)

Reported by a physician from France on 2007-10-31

Patient: 36 year old male

Adverse reactions / side effects: Gastrointestinal Haemorrhage, Pneumoperitoneum, Disease Progression

Suspect drug(s):
Sutent (Sunitinib)

Other drugs received by patient: Other Analgesics and Antipyretics



Adverse event in female receiving Sutent (Sunitinib)

Reported by a individual with unspecified qualification from United States on 2007-10-31

Patient: female, weighing 56.2 kg (123.6 pounds)

Adverse reactions / side effects: Cellulitis

Adverse event resulted in: hospitalization

Suspect drug(s):
Paclitaxel
    Indication: Breast Cancer

Sutent
    Administration route: Oral
    Indication: Breast Cancer

Other drugs received by patient: Procrit; Procrit; Senokot; Prilosec; Motrin; Lyrica



Adverse event in female receiving Sutent (Sunitinib)

Reported by a physician from Australia on 2007-10-31

Patient: female, weighing 51.0 kg (112.2 pounds)

Adverse reactions / side effects: Death

Adverse event resulted in: death

Suspect drug(s):
Sutent (Sunitinib)

Other drugs received by patient: Alendronate Sodium; Atenolol; Mobic; Simvastatin



Adverse event in female receiving Sutent (Sunitinib)

Reported by a individual with unspecified qualification from Germany on 2007-10-30

Patient: female, weighing 76.0 kg (167.2 pounds)

Adverse reactions / side effects: Haematuria, Renal Cell Carcinoma Stage Unspecified, Disease Progression

Adverse event resulted in: death, hospitalization

Suspect drug(s):
Sutent
    Administration route: Oral
    Indication: Renal Cell Carcinoma Stage Unspecified

Sutent
    Indication: Metastatic Renal Cell Carcinoma

Other drugs received by patient: Lercanidipine; Cynt; Metoprolol; Combaren; Morphine Sulfate; Omeprazole; Aspirin; Oxygesic; Ibuprofen; Sevredol



Adverse event in male receiving Sutent (Sunitinib)

Reported by a individual with unspecified qualification from United States on 2007-10-30

Patient: male, weighing 69.0 kg (151.8 pounds)

Adverse reactions / side effects: Back Pain, Myalgia, Pain in Extremity, Pyrexia

Adverse event resulted in: hospitalization

Suspect drug(s):
Sutent
    Administration route: Oral
    Indication: Renal Cell Carcinoma Stage Unspecified

Xeloda
    Administration route: Oral
    Indication: Renal Cell Carcinoma Stage Unspecified
    Start date: 2005-05-24
    End date: 2005-06-19

Other drugs received by patient: Protonix; Zoloft; Colace; Vitamin B6; Mylanta; Mylanta; Magic Mouthwash; Cortef; Fludrocortisone Acetate



Adverse event in male receiving Sutent (Sunitinib)

Reported by a physician from Australia on 2007-10-30

Patient: male

Adverse reactions / side effects: Renal Cell Carcinoma Stage Unspecified, Pathological Fracture, Disease Progression

Adverse event resulted in: hospitalization

Suspect drug(s):
Sutent (Sunitinib)



Adverse event in male receiving Sutent (Sunitinib)

Reported by a individual with unspecified qualification from Argentina on 2007-10-30

Patient: male, weighing 70.0 kg (154.0 pounds)

Adverse reactions / side effects: Performance Status Decreased, Anaemia

Suspect drug(s):
Sutent (Sunitinib)

Other drugs received by patient: Amino Acids; Megestrol Acetate



Adverse event in female receiving Sutent (Sunitinib)

Reported by a individual with unspecified qualification on 2007-10-30

Patient: female, weighing 74.3 kg (163.5 pounds)

Adverse reactions / side effects: Dyspnoea Exertional

Adverse event resulted in: hospitalization

Suspect drug(s):
Sutent (Sunitinib)

Other drugs received by patient: Lovenox; Percocet; Synthroid



Adverse event in female receiving Sutent (Sunitinib)

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

Patient: female

Adverse reactions / side effects: Death, Haemorrhage

Adverse event resulted in: death, hospitalization

Suspect drug(s):
Sutent (Sunitinib)



Adverse event in male receiving Sutent (Sunitinib)

Reported by a physician from Australia on 2007-10-30

Patient: male, weighing 69.0 kg (151.8 pounds)

Adverse reactions / side effects: Death

Adverse event resulted in: death

Suspect drug(s):
Sutent (Sunitinib)

Other drugs received by patient: Rabeprazole Sodium; Allopurinol; Levothyroxine Sodium; Acetaminophen; Tenopt; Xalatan



Adverse event in male receiving Sutent (Sunitinib)

Reported by a individual with unspecified qualification from United States on 2007-10-30

Patient: male, weighing 71.3 kg (156.9 pounds)

Adverse reactions / side effects: Upper Gastrointestinal Haemorrhage, Bradycardia

Adverse event resulted in: death, hospitalization

Suspect drug(s):
Sutent (Sunitinib)

Other drugs received by patient: Lovenox; Levothyroxine Sodium; Omeprazole; Methylin; Neurontin; Zofran; Requip; Atrovent; Senna; Acetaminophen W / Codeine



Adverse event in 64 year old male receiving Sutent (Sunitinib)

Reported by a individual with unspecified qualification from Argentina on 2007-10-30

Patient: 64 year old male, weighing 95.0 kg (209.0 pounds)

Adverse reactions / side effects: Jaundice, Hypertension

Suspect drug(s):
Sutent (Sunitinib)

Other drugs received by patient: Antihypertensives



Adverse event in male receiving Sutent (Sunitinib)

Reported by a individual with unspecified qualification from India on 2007-10-29

Patient: male, weighing 60.0 kg (132.0 pounds)

Adverse reactions / side effects: Death, Hypothyroidism, Thrombocytopenia

Adverse event resulted in: death, hospitalization

Suspect drug(s):
Sutent (Sunitinib)



Adverse event in male receiving Sutent (Sunitinib)

Reported by a physician from Germany on 2007-10-29

Patient: male

Adverse reactions / side effects: Blood Alkaline Phosphatase Increased, Gamma-Glutamyltransferase Increased, Skin Discolouration, Aspartate Aminotransferase Increased, Alanine Aminotransferase Increased, Thyroid Function Test Abnormal

Suspect drug(s):
Sutent (Sunitinib)



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

Reported by a individual with unspecified qualification from United States on 2007-10-29

Patient: 56 year old female, weighing 36.1 kg (79.4 pounds)

Adverse reactions / side effects: Tumour Haemorrhage

Adverse event resulted in: death, hospitalization

Suspect drug(s):
Sutent (Sunitinib)



Adverse event in female receiving Sutent (Sunitinib)

Reported by a physician from Mexico on 2007-10-29

Patient: female

Adverse reactions / side effects: Yellow Skin, Personality Disorder

Suspect drug(s):
Sutent (Sunitinib)



Adverse event in female receiving Sutent (Sunitinib)

Reported by a individual with unspecified qualification from United States on 2007-10-29

Patient: female, weighing 61.2 kg (134.6 pounds)

Adverse reactions / side effects: Dyspnoea, Oedema Peripheral, Hypoxia

Adverse event resulted in: hospitalization

Suspect drug(s):
Paclitaxel
    Indication: Breast Cancer
    Start date: 2006-10-17
    End date: 2006-11-27

Sutent
    Administration route: Oral
    Indication: Breast Cancer
    Start date: 2006-10-18
    End date: 2006-11-14

Sutent
    Administration route: Oral
    Start date: 2006-11-15
    End date: 2006-12-08

Other drugs received by patient: Vitamin CAP; Selenium; Vitamin A; Capsaicin; Ginkgo Biloba



Adverse event in female receiving Sutent (Sunitinib)

Reported by a individual with unspecified qualification from United States on 2007-10-29

Patient: female, weighing 63.8 kg (140.4 pounds)

Adverse reactions / side effects: Intestinal Fistula

Adverse event resulted in: hospitalization

Suspect drug(s):
Sutent
    Administration route: Oral
    Indication: Mueller's Mixed Tumour
    Start date: 2007-07-25
    End date: 2007-08-14

Sutent
    Administration route: Oral

Other drugs received by patient: Aldactazide; Ativan; Celexa; Folic Acid; Lipitor; Metformin HCL; Vitamin CAP; Prednisone; Zofran; Pyridoxine Hydrochloride

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