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Avastin (Bevacizumab) - Adverse Event Reports - Hospitalization

 



Index of reports > Cases resulting in hospitalization (515)

     Diarrhoea (42)Pyrexia (35)Nausea (33)Vomiting (31)Dehydration (28)Haemoglobin Decreased (26)Abdominal Pain (24)Dyspnoea (21)Asthenia (21)Sepsis (18)

Below is the selection of adverse event reports related to Avastin (Bevacizumab) that includes cases resulting in hospitalization.

 Reports 1 - 25 of 515   Next >>

Adverse event in female receiving Avastin (Bevacizumab)

Reported by a physician from United Kingdom on 2007-10-31

Patient: female, weighing 90.0 kg (198.0 pounds)

Adverse reactions / side effects: Uveitis

Adverse event resulted in: hospitalization

Suspect drug(s):
Avastin (Bevacizumab)



Adverse event in female receiving Avastin (Bevacizumab)

Reported by a consumer/non-health professional from United States on 2007-10-31

Patient: female, weighing 56.0 kg (123.2 pounds)

Adverse reactions / side effects: Blood Pressure Increased, Body Temperature Increased, Post Procedural Complication, Headache, Hydrocephalus, Meningitis, Cerebrospinal Fistula, Intracranial Hypotension

Adverse event resulted in: hospitalization

Suspect drug(s):
Tarceva
    Dosage: 200 mg
    Indication: Glioblastoma Multiforme
    Start date: 2007-04-13

Avastin
    Dosage: 10 mg/kg
    Indication: Glioblastoma Multiforme
    Start date: 2007-04-13

Other drugs received by patient: Lexapro; Keppra; Decadron; Lipitor



Adverse event in female receiving Avastin (Bevacizumab)

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

Patient: female, weighing 50.0 kg (110.0 pounds)

Adverse reactions / side effects: Uveitis

Adverse event resulted in: hospitalization

Suspect drug(s):
Avastin (Bevacizumab)



Adverse event in male receiving Avastin (Bevacizumab)

Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-29

Patient: male, weighing 175.0 kg (385.0 pounds)

Adverse reactions / side effects: Hepatic Failure, Disease Progression

Adverse event resulted in: hospitalization

Suspect drug(s):
Avastin
    Dosage: 590 mg, unk
    Indication: Metastatic Neoplasm
    Start date: 2005-07-18
    End date: 2005-08-02

Aranesp
    Dosage: 200 a?g, prn
    Indication: Anaemia

Oxaliplatin
    Dosage: 160 mg, unk
    Indication: Metastatic Neoplasm
    Start date: 2005-07-18
    End date: 2005-08-02

Leucovorin
    Dosage: 380 mg, unk
    Indication: Metastatic Neoplasm
    Start date: 2005-07-18
    End date: 2005-08-03

Fluorouracil
    Dosage: 1140 mg, unk
    Indication: Metastatic Neoplasm
    Start date: 2005-07-18
    End date: 2005-07-20

Fluorouracil
    Dosage: 760 mg, unk
    Start date: 2005-08-02
    End date: 2005-08-03

Fluorouracil
    Dosage: 1140 mg, unk
    Start date: 2005-08-02
    End date: 2005-08-04



Adverse event in female receiving Avastin (Bevacizumab)

Reported by a consumer/non-health professional from United States on 2007-10-26

Patient: female

Adverse reactions / side effects: Small Intestinal Obstruction, Neoplasm Progression

Adverse event resulted in: hospitalization

Suspect drug(s):
Avastin (Bevacizumab)

Other drugs received by patient: Folinic Acid; Fluorouracil; Oxaliplatin



Adverse event in female receiving Avastin (Bevacizumab)

Reported by a consumer/non-health professional from United States on 2007-10-26

Patient: female

Adverse reactions / side effects: Coronary Artery Thrombosis, Pulmonary Thrombosis

Adverse event resulted in: hospitalization

Suspect drug(s):
Avastin (Bevacizumab)



Adverse event in 68 year old female receiving Avastin (Bevacizumab)

Reported by a health professional (non-physician/pharmacist) from Japan on 2007-10-26

Patient: 68 year old female

Adverse reactions / side effects: Gastric Ulcer Haemorrhage, Pyrexia

Adverse event resulted in: hospitalization

Suspect drug(s):
Taxol
    Indication: non-Small Cell Lung Cancer Metastatic
    Start date: 2007-08-01
    End date: 2007-10-10

Paraplatin
    Indication: non-Small Cell Lung Cancer Metastatic
    Start date: 2007-08-01
    End date: 2007-10-10

Avastin
    Indication: non-Small Cell Lung Cancer Metastatic
    Start date: 2007-08-01
    End date: 2007-09-14

Other drugs received by patient: Durotep; Primperan; Kenalog; Novamin; Loxonin; Selbex; Adofeed; Oxynorm; Goshajinkigan; Senna Leaf; Oxycontin; Magmitt; Noritren; Laxoberon



Adverse event in male receiving Avastin (Bevacizumab)

Reported by a consumer/non-health professional from United Kingdom on 2007-10-26

Patient: male

Adverse reactions / side effects: Pancytopenia, Septic Shock

Adverse event resulted in: death, hospitalization

Suspect drug(s):
Avastin
    Dosage: 275 mg, unk
    Indication: Colorectal Cancer
    Start date: 2006-07-10
    End date: 2006-07-10

Folinic Acid
    Indication: Drug USE FOR Unknown Indication
    Start date: 2006-07-10
    End date: 2006-07-10

Fluorouracil
    Dosage: 4600 mg, unk
    Indication: Colorectal Cancer
    Start date: 2006-07-10
    End date: 2006-07-10

Camptosar
    Dosage: 300 mg, unk
    Indication: Colorectal Cancer
    Start date: 2006-07-10
    End date: 2006-07-10



Adverse event in 79 year old female receiving Avastin (Bevacizumab)

Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-25

Patient: 79 year old female, weighing 80.3 kg (176.6 pounds)

Adverse reactions / side effects: Osteonecrosis

Adverse event resulted in: hospitalization, disablity

Suspect drug(s):
Avastin (Bevacizumab)

Other drugs received by patient: Paclitaxel; Carboplatin; Synthroid; Sinemet; Actos; Lasix; Percocet; Betoptic; Protonix; Colace; Senokot; Coumadin; Dilaudid



Adverse event in female receiving Avastin (Bevacizumab)

Reported by a physician from United States on 2007-10-25

Patient: female

Adverse reactions / side effects: Body Temperature Increased

Adverse event resulted in: hospitalization

Suspect drug(s):
Avastin
    Dosage: 1047 mg, unk
    Indication: non-Small Cell Lung Cancer
    Start date: 2007-09-24

Rshapo2l-Trail
    Dosage: 1400 mg, unk
    Indication: non-Small Cell Lung Cancer
    Start date: 2007-09-24



Adverse event in female receiving Avastin (Bevacizumab)

Reported by a physician from United Kingdom on 2007-10-25

Patient: female

Adverse reactions / side effects: Anaemia

Adverse event resulted in: hospitalization

Suspect drug(s):
Avastin (Bevacizumab)

Other drugs received by patient: Duroferon; Fosamax; Burinex; Vitamin B-12; Maxitrol



Adverse event in 68 year old female receiving Avastin (Bevacizumab)

Reported by a health professional (non-physician/pharmacist) from Japan on 2007-10-24

Patient: 68 year old female

Adverse reactions / side effects: Pyrexia, Altered State of Consciousness

Adverse event resulted in: hospitalization

Suspect drug(s):
Taxol
    Indication: non-Small Cell Lung Cancer Metastatic
    Start date: 2007-08-01
    End date: 2007-10-10

Paraplatin
    Indication: non-Small Cell Lung Cancer Metastatic
    Start date: 2007-08-01
    End date: 2007-10-10

Avastin
    Indication: non-Small Cell Lung Cancer Metastatic
    Start date: 2007-08-01
    End date: 2007-09-14

Other drugs received by patient: Durotep; Primperan; Kenalog; Novamin; Loxonin; Selbex; Adofeed; Oxynorm; Goshajinkigan; Senna Leaf; Oxycontin; Magmitt; Noritren; Laxoberon



Adverse event in female receiving Avastin (Bevacizumab)

Reported by a physician from United Kingdom on 2007-10-24

Patient: female

Adverse reactions / side effects: Gastrointestinal Perforation, Intestinal Ischaemia, Nausea, Diarrhoea, General Physical Health Deterioration

Adverse event resulted in: hospitalization

Suspect drug(s):
Avastin (Bevacizumab)

Other drugs received by patient: Taxotere



Adverse event in 76 year old female receiving Avastin (Bevacizumab)

Reported by a pharmacist from United States on 2007-10-24

Patient: 76 year old female, weighing 60.9 kg (134.0 pounds)

Adverse reactions / side effects: Confusional State

Adverse event resulted in: hospitalization

Suspect drug(s):
Avastin (Bevacizumab)



Adverse event in male receiving Avastin (Bevacizumab)

Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-23

Patient: male, weighing 175.0 kg (385.0 pounds)

Adverse reactions / side effects: Abdominal Pain, Jaundice, Metastatic Neoplasm, Bile Duct Obstruction, Malignant Neoplasm Progression, Hepatic Failure, Oedema Peripheral, Abdominal Distension, Decreased Appetite, Lethargy

Adverse event resulted in: death, hospitalization

Suspect drug(s):
Fluorouracil
    Indication: Metastatic Neoplasm
    Start date: 2005-08-02
    End date: 2005-08-04

Leucovorin
    Indication: Metastatic Neoplasm
    Start date: 2005-08-02
    End date: 2005-08-03

Oxaliplatin
    Indication: Metastatic Neoplasm
    Start date: 2005-08-02
    End date: 2005-08-02

Aranesp
    Indication: Anaemia

Avastin
    Indication: Metastatic Neoplasm
    Start date: 2005-08-02
    End date: 2005-08-02

Avastin
    Dosage: unk



Adverse event in male receiving Avastin (Bevacizumab)

Reported by a consumer/non-health professional from United States on 2007-10-23

Patient: male, weighing 99.8 kg (219.5 pounds)

Adverse reactions / side effects: Cerebrovascular Accident

Adverse event resulted in: hospitalization

Suspect drug(s):
Avastin
    Dosage: 0.5 mg, 1/month
    Indication: Macular Degeneration
    Start date: 2006-07-20

Lucentis
    Dosage: 500 a?g, unk
    Indication: Macular Degeneration
    Start date: 2006-10-19



Adverse event in female receiving Avastin (Bevacizumab)

Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-19

Patient: female, weighing 78.1 kg (171.8 pounds)

Adverse reactions / side effects: Fluid Overload

Adverse event resulted in: hospitalization

Suspect drug(s):
Avastin
    Dosage: 15 mg/kg, q3w
    Indication: non-Small Cell Lung Cancer
    Start date: 2007-09-19

Tarceva
    Dosage: 150 mg, qd
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication
    Start date: 2007-09-19
    End date: 2007-10-03

Other drugs received by patient: 0.9% NS



Adverse event in 53 year old male receiving Avastin (Bevacizumab)

Reported by a physician from United States on 2007-10-19

Patient: 53 year old male

Adverse reactions / side effects: Respiratory Failure

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Avastin (Bevacizumab)

Other drugs received by patient: Synthroid; Oxaliplatin; Fluorouracil; Leucovorin



Adverse event in female receiving Avastin (Bevacizumab)

Reported by a physician from United Kingdom on 2007-10-18

Patient: female

Adverse reactions / side effects: Dysphagia, Dysphonia

Adverse event resulted in: hospitalization

Suspect drug(s):
Avastin (Bevacizumab)

Other drugs received by patient: Taxol



Adverse event in 76 year old female receiving Avastin (Bevacizumab)

Reported by a pharmacist from United States on 2007-10-18

Patient: 76 year old female, weighing 61.0 kg (134.2 pounds)

Adverse reactions / side effects: Claustrophobia, Respiratory Rate Increased, Global Amnesia, Cerebrovascular Accident, Macular Degeneration, Tremor, Speech Disorder, Reversible Posterior Leukoencephalopathy Syndrome, Balance Disorder, Clumsiness, Dizziness, Memory Impairment

Adverse event resulted in: hospitalization

Suspect drug(s):
Avastin (Bevacizumab)



Adverse event in 59 year old male receiving Avastin (Bevacizumab)

Reported by a pharmacist from United States on 2007-10-18

Patient: 59 year old male, weighing 82.0 kg (180.4 pounds)

Adverse reactions / side effects: Pancreatitis

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Erbitux
    Indication: Colon Cancer Metastatic
    Start date: 2006-11-22
    End date: 2007-05-19

Avastin
    Indication: Colon Cancer Metastatic
    Start date: 2006-12-20
    End date: 2007-09-05

Other drugs received by patient: CPT-11; Magnesium Sulfate; Benadryl



Adverse event in 40 year old female receiving Avastin (Bevacizumab)

Reported by a health professional (non-physician/pharmacist) from Japan on 2007-10-18

Patient: 40 year old female

Adverse reactions / side effects: Fatigue, Anorexia, Myocardial Infarction

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Taxol
    Dosage: 6th cycle was started on 28-sep-oct.
    Indication: non-Small Cell Lung Cancer
    Start date: 2007-06-01
    End date: 2007-09-28

Paraplatin
    Dosage: 6th cycle was started on 28-sep-2007
    Indication: non-Small Cell Lung Cancer
    Start date: 2007-06-01
    End date: 2007-09-28

Avastin
    Dosage: 6th cycle was started on 27-sep-2007
    Indication: non-Small Cell Lung Cancer
    Start date: 2007-06-01
    End date: 2007-09-28



Adverse event in female receiving Avastin (Bevacizumab)

Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-10-18

Patient: female

Adverse reactions / side effects: Confusional State, Aphasia, Dizziness, Transient Ischaemic Attack

Adverse event resulted in: hospitalization

Suspect drug(s):
Avastin (Bevacizumab)

Other drugs received by patient: Eutirox



Adverse event in female receiving Avastin (Bevacizumab)

Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-18

Patient: female, weighing 61.2 kg (134.7 pounds)

Adverse reactions / side effects: Abdominal Pain, Abdominal Abscess, Appendicectomy

Adverse event resulted in: hospitalization

Suspect drug(s):
Avastin (Bevacizumab)

Other drugs received by patient: Taxol



Adverse event in male receiving Avastin (Bevacizumab)

Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-10-17

Patient: male, weighing 79.5 kg (174.9 pounds)

Adverse reactions / side effects: Malaise, Creutzfeldt-Jakob Disease, Convulsion

Adverse event resulted in: death, hospitalization

Suspect drug(s):
Avastin
    Dosage: unk, single
    Indication: Drug USE FOR Unknown Indication
    Start date: 2007-01-22
    End date: 2007-01-22

Lucentis
    Dosage: unk, 1/month
    Indication: Drug USE FOR Unknown Indication
    Start date: 2007-01-01
    End date: 2007-05-01

Other drugs received by patient: Pravastatin; Quinapril HCL; Ranitidine HCL; Caltrate + D



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