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This is an index of adverse event reports related to Taxol (Paclitaxel). 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 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 (637)
Cases resulting in a serious event (575)
Cases resulting in death (93)
Cases resulting in life threatening events (54)
Cases resulting in hospitalization (385)
Cases resulting in disability (36)
Cases resulting in other serious reactions (145)
Below is a sample of adverse event reports reports related to Taxol (Paclitaxel). For a complete list and/or a specific selection of reports, please use the links in the index above.
Adverse event in female receiving Taxol (Paclitaxel)
Reported by a individual with unspecified qualification from United States on 2007-10-31
Patient: female, weighing 68.4 kg (150.5 pounds)
Adverse reactions / side effects: Blood Urine Present, Vaginal Discharge, Constipation, Ascites, Peritonitis
Adverse event resulted in: hospitalization
Suspect drug(s):
Carboplatin
Dosage: 656 mg
End date: 2007-10-09
Taxol
Dosage: 310 mg
Adverse event in 52 year old female receiving Taxol (Paclitaxel)
Reported by a physician from Japan on 2007-10-31
Patient: 52 year old female
Adverse reactions / side effects: Hypertension, Loss of Consciousness
Adverse event resulted in: hospitalization
Suspect drug(s):
Taxol (Paclitaxel)
Other drugs received by patient: Oxycontin; Norvasc; Durotep; Opso; Zantac; Decadron; Restamin; TS-1
Adverse event in female receiving Taxol (Paclitaxel)
Reported by a individual with unspecified qualification from United States on 2007-10-30
Patient: female, weighing 67.4 kg (148.3 pounds)
Adverse reactions / side effects: Pruritus, Tachycardia, Hypotension, Infusion Related Reaction
Adverse event resulted in: hospitalization
Suspect drug(s):
Taxol (Paclitaxel)
Adverse event in 41 year old male receiving Taxol (Paclitaxel)
Reported by a physician from Japan on 2007-10-30
Patient: 41 year old male
Adverse reactions / side effects: Pancytopenia, Renal Failure Acute
Adverse event resulted in: death
Suspect drug(s):
Taxol
Indication: Lung Adenocarcinoma
Start date: 2007-10-03
End date: 2007-10-03
Paraplatin
Indication: Lung Adenocarcinoma
Start date: 2007-10-03
End date: 2007-10-03
Adverse event in 55 year old female receiving Taxol (Paclitaxel)
Reported by a physician from Japan on 2007-10-29
Patient: 55 year old female
Adverse reactions / side effects: Myelodysplastic Syndrome
Adverse event resulted in: hospitalization
Suspect drug(s):
Taxol
Dosage: 22 cycles of treatment(10 taxol+paraplatin combination therapy) and 12 cycles of taxol monotherapy.
Indication: Ovarian Cancer
Start date: 2005-10-18
End date: 2007-05-11
Paraplatin
Indication: Ovarian Cancer
Start date: 2005-10-18
End date: 2006-06-02
Other drugs received by patient: Orgadrone; Famotidine
Adverse event in 25 year old female receiving Taxol (Paclitaxel)
Reported by a physician from Japan on 2007-10-29
Patient: 25 year old female
Adverse reactions / side effects: Myalgia, Visual Acuity Reduced
Adverse event resulted in: disablity
Suspect drug(s):
Taxol (Paclitaxel)
Adverse event in female receiving Taxol (Paclitaxel)
Reported by a individual with unspecified qualification from United States on 2007-10-29
Patient: female, weighing 62.7 kg (138.0 pounds)
Adverse reactions / side effects: Neutrophil Count Increased, Blood Chloride Decreased, Fall, Haemoglobin Decreased, Haematocrit Decreased, Aspartate Aminotransferase Increased, Dizziness, Blood Sodium Decreased, Hypovolaemia, Decreased Appetite
Adverse event resulted in: hospitalization
Suspect drug(s):
Carboplatin
Dosage: 686 mg
Taxol
Dosage: 287 mg
Adverse event in female receiving Taxol (Paclitaxel)
Reported by a consumer/non-health professional from Denmark on 2007-10-26
Patient: female
Adverse reactions / side effects: Pulmonary Fibrosis
Adverse event resulted in: disablity
Suspect drug(s):
Carboplatin
Indication: Ovarian Cancer
Start date: 2006-07-19
End date: 2006-11-01
Taxol
Indication: Ovarian Cancer
Start date: 2006-07-19
End date: 2006-11-01
Adverse event in 68 year old female receiving Taxol (Paclitaxel)
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 Taxol (Paclitaxel)
Reported by a individual with unspecified qualification from United States on 2007-10-26
Patient: male, weighing 74.3 kg (163.5 pounds)
Adverse reactions / side effects: Pneumothorax, Pyrexia, Respiratory Distress, Lung Abscess
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Carboplatin
Dosage: 6 mg
Taxol
Dosage: 200 mg
Other drugs received by patient: Albuterol; Calcium; Ertapenem; Heparin; Hydrocodone Bitartrate; Ipratropium Bromide; Mirtazapine; Omeprazole; Oxycodone HCL; Senna; Vitamin D; Voriconazole
Adverse event in female receiving Taxol (Paclitaxel)
Reported by a individual with unspecified qualification from United States on 2007-10-26
Patient: female, weighing 83.7 kg (184.1 pounds)
Adverse reactions / side effects: Chills, Pyrexia, Hyperhidrosis
Adverse event resulted in: hospitalization
Suspect drug(s):
Cisplatin
Dosage: 97 mg
Doxorubicin Hydrochloride
Dosage: 90 mg
G-CSF (Filgrastim, Amgen)
Dosage: 480 mcg
Taxol
Dosage: 310 mg
Other drugs received by patient: Diovan; Glimepiride; Metformin HCL
Adverse event in 52 year old female receiving Taxol (Paclitaxel)
Reported by a physician from Japan on 2007-10-26
Patient: 52 year old female
Adverse reactions / side effects: Hypertension, Loss of Consciousness
Adverse event resulted in: hospitalization
Suspect drug(s):
Taxol (Paclitaxel)
Other drugs received by patient: Oxycontin; Norvasc; Durotep; Opso; Zantac; Decadron; Restamin; TS-1
Adverse event in female receiving Taxol (Paclitaxel)
Reported by a physician from Japan on 2007-10-25
Patient: female
Adverse reactions / side effects: Myelodysplastic Syndrome
Adverse event resulted in: hospitalization
Suspect drug(s):
Taxol
Indication: Ovarian Cancer
Paraplatin
Indication: Ovarian Cancer
Adverse event in female receiving Taxol (Paclitaxel)
Reported by a individual with unspecified qualification from United States on 2007-10-25
Patient: female, weighing 66.0 kg (145.2 pounds)
Adverse reactions / side effects: Neutrophil Count Decreased
Suspect drug(s):
Carboplatin
Dosage: 600 mg
Taxol
Dosage: 290 mg
Other drugs received by patient: Aspirin; Compazine; Decadron
Adverse event in 68 year old female receiving Taxol (Paclitaxel)
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 65 year old female receiving Taxol (Paclitaxel)
Reported by a health professional (non-physician/pharmacist) from Germany on 2007-10-24
Patient: 65 year old female, weighing 68.0 kg (149.6 pounds)
Adverse reactions / side effects: Febrile Neutropenia
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Taxol
Indication: Breast Cancer
Start date: 2007-09-11
Epirubicin
Indication: Breast Cancer
Start date: 2007-07-30
End date: 2007-08-28
Other drugs received by patient: Zolpidem Tartrate; Neorecormon; Neulasta
Adverse event in 61 year old female receiving Taxol (Paclitaxel)
Reported by a physician from France on 2007-10-24
Patient: 61 year old female
Adverse reactions / side effects: Hepatitis Fulminant
Adverse event resulted in: death
Suspect drug(s):
Taxol
Start date: 2007-10-11
Carboplatin
Taxotere
Avastin
Start date: 2007-10-11
Solu-Medrol
Start date: 2007-10-11
Arimidex
Administration route: Oral
Start date: 2007-10-11
Adverse event in 26 year old female receiving Taxol (Paclitaxel)
Reported by a physician from Italy on 2007-10-23
Patient: 26 year old female, weighing 68.0 kg (149.6 pounds)
Adverse reactions / side effects: Dyspnoea, Anaphylactic Reaction, Tachycardia, Hyperhidrosis, Abdominal Pain Upper
Adverse event resulted in: life threatening event
Suspect drug(s):
Taxol
Dosage: 140mg weekly
Indication: Breast Cancer
Start date: 2007-07-20
End date: 2007-07-20
Trastuzumab
Indication: Breast Cancer
Other drugs received by patient: Vinorelbine
Adverse event in receiving Taxol (Paclitaxel)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-23
Patient:
Adverse reactions / side effects: Haemoglobin Decreased, Atelectasis, Haematocrit Decreased, Dyspnoea, Pneumonia, Chest Pain, Myocardial Infarction, Blood Glucose Increased
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Methadone HCL
Dosage: 10 mg, 1-2 tablet, q6hr
Administration route: Oral
Indication: Pain
Methadone HCL
Dosage: 40 mg, bid
Administration route: Oral
Start date: 2007-08-20
CP-751,871
Dosage: 1560 mg, single (1 dose q 21 days)
Indication: non-Small Cell Lung Cancer
Start date: 2007-06-20
End date: 2007-06-20
CP-751,871
Dosage: 1600 mg, single (1 dose q 21 days)
Start date: 2007-07-11
End date: 2007-07-11
CP-751,871
Dosage: 1540 mg, single (1 dose q 21 days)
Start date: 2007-08-01
Taxol
Dosage: 395 mg, single (1 dose q 21 days)
Indication: non-Small Cell Lung Cancer
Start date: 2007-06-19
End date: 2007-06-19
Taxol
Dosage: 382 mg, single (1 dose q 21 days)
Start date: 2007-07-10
End date: 2007-07-10
Taxol
Dosage: 329 mg, single (1 dose q 21 days)
Start date: 2007-07-31
End date: 2007-07-31
Carboplatin
Dosage: 620 mg, single (1 dose q 21 days)
Indication: non-Small Cell Lung Cancer
Start date: 2007-06-19
End date: 2007-06-19
Carboplatin
Dosage: 564 mg, single ( 1 dose q 21 days)
Start date: 2007-07-10
End date: 2007-07-10
Carboplatin
Dosage: 516 mg, single (1 dose q 21 days)
Start date: 2007-07-31
Lexapro
Dosage: 10 mg, qd
Administration route: Oral
Start date: 2007-06-12
Coumadin
Dosage: 5 mg, qd
Administration route: Oral
Start date: 2007-07-31
Lovenox
Dosage: 10 mg, q6-8hr
Administration route: Oral
Start date: 2007-06-12
Other drugs received by patient: Reglan / 00041901 /; Nitroglycerin; Gabapentin; Oxycodone HCL
Adverse event in 41 year old male receiving Taxol (Paclitaxel)
Reported by a physician from Japan on 2007-10-22
Patient: 41 year old male
Adverse reactions / side effects: Renal Failure Acute
Adverse event resulted in: death
Suspect drug(s):
Taxol
Indication: non-Small Cell Lung Cancer
Start date: 2007-10-03
End date: 2007-10-03
Paraplatin
Indication: non-Small Cell Lung Cancer
Start date: 2007-10-03
End date: 2007-10-03
Adverse event in 61 year old female receiving Taxol (Paclitaxel)
Reported by a consumer/non-health professional from Japan on 2007-10-22
Patient: 61 year old female
Adverse reactions / side effects: Acute Myelomonocytic Leukaemia
Adverse event resulted in: hospitalization
Suspect drug(s):
Taxol
Indication: Breast Cancer
Radiotherapy
Indication: Breast Cancer
Adverse event in female receiving Taxol (Paclitaxel)
Reported by a individual with unspecified qualification from United States on 2007-10-22
Patient: female, weighing 109.0 kg (239.8 pounds)
Adverse reactions / side effects: Oral Intake Reduced, Vomiting, Nausea, Hypotension, Febrile Neutropenia, Culture Urine Positive, Convulsion, Fungal Infection, Blood Culture Positive, Catheter Sepsis, Escherichia Infection, White Blood Cell Count Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Cisplatin
Dosage: 100 mg
Doxorubicin Hydrochloride
Dosage: 90 mg
Taxol
Dosage: 320 mg
Adverse event in 65 year old female receiving Taxol (Paclitaxel)
Reported by a consumer/non-health professional from United States on 2007-10-22
Patient: 65 year old female, weighing 77.1 kg (169.6 pounds)
Adverse reactions / side effects: Breast Pain, Dyspnoea, Malaise, Pruritus, Complication of Device Insertion, Fear, Wheezing
Suspect drug(s):
Cypher Drug Eluting Stent Johnson and Johnson
Indication: Coronary Artery Occlusion
Start date: 2004-08-14
End date: 2007-10-21
Taxol
Indication: Coronary Arterial Stent Insertion
Start date: 2004-12-09
End date: 2007-10-21
Adverse event in 64 year old female receiving Taxol (Paclitaxel)
Reported by a physician from Japan on 2007-10-22
Patient: 64 year old female
Adverse reactions / side effects: Erythema Nodosum
Adverse event resulted in: disablity
Suspect drug(s):
Taxol
Indication: Ovarian Cancer
Start date: 2007-08-28
End date: 2007-08-28
Paraplatin
Indication: Ovarian Cancer
Start date: 2007-08-28
End date: 2007-08-28
Adverse event in 52 year old female receiving Taxol (Paclitaxel)
Reported by a physician from Japan on 2007-10-19
Patient: 52 year old female
Adverse reactions / side effects: Blood Pressure Increased, Flushing, Hyperhidrosis, Delirium
Adverse event resulted in: hospitalization
Suspect drug(s):
Taxol (Paclitaxel)
Other drugs received by patient: Decadron; Zantac; Diphenhydramine HCL; Oxycontin
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