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Fluorouracil (Fluorouracil) - Reports of Side Effects & Adverse Reactions

 


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This is an index of adverse event reports related to Fluorouracil. 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 (530)
     Vomiting (39)Diarrhoea (39)Abdominal Pain (30)more >>

Cases resulting in a serious event (505)
     Vomiting (39)Diarrhoea (38)Abdominal Pain (30)more >>

Cases resulting in death (100)
     Vomiting (8)Cardiac Failure (8)Abdominal Pain (7)more >>

Cases resulting in life threatening events (40)
     Pyrexia (5)Abdominal Pain (4)Dyspnoea (4)more >>

Cases resulting in hospitalization (334)
     Vomiting (34)Diarrhoea (31)Abdominal Pain (26)more >>

Cases resulting in disability (9)
     Back Pain (2)Bile Duct Obstruction (2)Metastases TO Liver (2)more >>

Cases resulting in other serious reactions (140)
     Neoplasm Recurrence (10)Stomatitis (9)Acute Myeloid Leukaemia (8)more >>

Below is a sample of adverse event reports reports related to Fluorouracil. For a complete list and/or a specific selection of reports, please use the links in the index above.

Adverse event in male receiving Fluorouracil

Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-31

Patient: male, weighing 100.9 kg (222.0 pounds)

Adverse reactions / side effects: Oral Intake Reduced, Clostridium Difficile Colitis

Adverse event resulted in: hospitalization

Suspect drug(s):
Cisplatin
    Dosage: 150mg iv
    Indication: Neoplasm Malignant
    Start date: 2007-08-23

Fluorouracil
    Dosage: 1500mg bid iv qd
    Indication: Neoplasm Malignant
    Start date: 2007-08-23
    End date: 2007-08-27

Taxotere
    Dosage: 150mg iv
    Indication: Neoplasm Malignant
    Start date: 2007-08-23

Other drugs received by patient: Ambien; Aspirin; Ativan; Compazine; Hyzaar; Lidex; Lipitor; Loprox; Nasonex; Singulair; Zofran



Adverse event in female receiving Fluorouracil

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

Patient: female, weighing 61.5 kg (135.3 pounds)

Adverse reactions / side effects: Vomiting, Diarrhoea, Hypokalaemia

Adverse event resulted in: hospitalization

Suspect drug(s):
Bevacizumab
    Dosage: 326 mg, q2w
    Indication: Colon Cancer
    Start date: 2007-04-04

Fluorouracil
    Dosage: 650 mg, q2w
    Start date: 2007-04-04

Leucovorin
    Dosage: 320 mg, q2w
    Indication: Colon Cancer
    Start date: 2007-04-04

Oxaliplatin
    Dosage: 137 mg, q2w
    Indication: Colon Cancer
    Start date: 2007-04-04

Other drugs received by patient: Rabeprazole Sodium; Zofran; Prochlorperazine; Aluminum Hydroxide Gel; Norvasc; Bisoprolol Fumarate; Ramipril



Adverse event in male receiving Fluorouracil

Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-31

Patient: male, weighing 100.9 kg (222.0 pounds)

Adverse reactions / side effects: Syncope Vasovagal, Arteriospasm Coronary, Cardiac Disorder

Adverse event resulted in: hospitalization

Suspect drug(s):
Cisplatin
    Dosage: 150mg iv
    Indication: Neoplasm Malignant
    Start date: 2007-08-23

Fluorouracil
    Dosage: 1500mg bid iv qd
    Indication: Neoplasm Malignant
    Start date: 2007-08-23
    End date: 2007-08-27

Taxotere
    Dosage: 150mg iv
    Indication: Neoplasm Malignant
    Start date: 2007-08-23

Other drugs received by patient: Ambien; Aspirin; Ativan; Compazine; Hyzaar; Lidex; Lipitor; Loprox; Nasonex; Singulair; Zofran



Adverse event in 77 year old male receiving Fluorouracil

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

Patient: 77 year old male

Adverse reactions / side effects: Nephrotic Syndrome, Renal Failure Acute

Adverse event resulted in: hospitalization

Suspect drug(s):
Erbitux
    Indication: Colon Cancer
    Start date: 2006-08-10
    End date: 2007-02-13

Fluorouracil
    Dosage: no.of dosage=d1+d2
    Indication: Colon Cancer
    Start date: 2005-07-19
    End date: 2007-02-13

Irinotecan HCL
    Indication: Colon Cancer
    Start date: 2005-07-19
    End date: 2007-02-13

Leucovorin
    Dosage: no.of dosage=d1+d2
    Indication: Colon Cancer
    Start date: 2005-07-19
    End date: 2007-02-13

Other drugs received by patient: Penmix



Adverse event in male receiving Fluorouracil

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

Patient: male, weighing 69.1 kg (152.0 pounds)

Adverse reactions / side effects: Fatigue, Vomiting, Nausea, Rectal Tenesmus, Proctalgia

Adverse event resulted in: hospitalization

Suspect drug(s):
Bevacizumab(rhumab Vegf)
    Dosage: 1130 mg
    End date: 2007-09-11

Eloxatin
    Dosage: 479 mg
    End date: 2007-09-11

Fluorouracil
    Dosage: 12632 mg
    End date: 2007-09-11

Leucovorin Calcium
    Dosage: 2256 mg
    End date: 2007-09-11



Adverse event in female receiving Fluorouracil

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

Patient: female, weighing 65.0 kg (143.0 pounds)

Adverse reactions / side effects: Pneumonia, Pancytopenia

Adverse event resulted in: death, hospitalization

Suspect drug(s):
Fluorouracil
    Dosage: 400 mg/m2 bolus followed by 600 mg/m2 infusion
    Start date: 2006-12-18
    End date: 2006-12-19

Leucovorin
    Start date: 2006-12-18
    End date: 2006-12-19

Oxaliplatin
    Indication: Colon Cancer
    Start date: 2006-12-18
    End date: 2006-12-18



Adverse event in female receiving Fluorouracil

Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-30

Patient: female, weighing 80.3 kg (176.7 pounds)

Adverse reactions / side effects: Pancytopenia, Splenomegaly

Suspect drug(s):
Eloxatin
    Dosage: 85 mg/m2 every 2 weeks
    Indication: Colon Cancer
    Start date: 2006-02-07
    End date: 2006-02-07

Fluorouracil
    Dosage: 500 mg/m2 every week
    Indication: Colon Cancer
    Start date: 2006-02-07
    End date: 2006-02-07

Leucovorin Calcium
    Dosage: 500 mg/m2 every week
    Indication: Colon Cancer
    Start date: 2006-02-07
    End date: 2006-02-07

Other drugs received by patient: Lomotil; Compazine; Iron Pill; Prozac



Adverse event in male receiving Fluorouracil

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

Patient: male, weighing 79.1 kg (174.0 pounds)

Adverse reactions / side effects: Type IV Hypersensitivity Reaction

Adverse event resulted in: hospitalization

Suspect drug(s):
Bevacizumab (Rhumab Vegf)
    Dosage: 387 mg
    End date: 2007-10-24

Eloxatin
    Dosage: 47 mg
    End date: 2007-10-24

Fluorouracil
    Dosage: 5180 mg
    End date: 2007-10-24

Leucovorin Calcium
    Dosage: 740 mg
    End date: 2007-10-24



Adverse event in male receiving Fluorouracil

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

Avastin
    Dosage: 590 mg, unk
    Indication: Metastatic Neoplasm
    Start date: 2005-07-18
    End date: 2005-08-02

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

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

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



Adverse event in female receiving Fluorouracil

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

Patient: female, weighing 52.7 kg (115.9 pounds)

Adverse reactions / side effects: Oral Intake Reduced, Intestinal Obstruction, Thirst

Adverse event resulted in: hospitalization

Suspect drug(s):
Bevacizumab (Rhumab Vegf)
    Dosage: 264 mg
    End date: 2007-10-10

Eloxatin
    Dosage: 128 mg
    End date: 2007-10-10

Fluorouracil
    Dosage: 4200 mg
    End date: 2007-10-12

Leucovorin Calcium
    Dosage: 600 mg
    End date: 2007-10-10



Adverse event in male receiving Fluorouracil

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

Camptosar
    Dosage: 300 mg, unk
    Indication: Colorectal Cancer
    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

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



Adverse event in 71 year old male receiving Fluorouracil

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

Patient: 71 year old male

Adverse reactions / side effects: Burning Sensation, Pruritus, Rash Maculo-Papular

Suspect drug(s):
Eloxatin
    Dosage: 166 mg

Fluorouracil
    Dosage: 780mg bolus/4680mg over 46?
    Start date: 2007-10-03

Other drugs received by patient: Leucovorin; Zofran; Decadron



Adverse event in female receiving Fluorouracil

Reported by a individual with unspecified qualification from United States on 2007-10-26

Patient: female, weighing 75.7 kg (166.5 pounds)

Adverse reactions / side effects: Neutropenia

Suspect drug(s):
Eloxatin
    Dosage: 150 mg

Fluorouracil
    Dosage: 4970 mg

Leucovorin Calcium
    Dosage: 700 mg



Adverse event in male receiving Fluorouracil

Reported by a physician from Germany on 2007-10-26

Patient: male

Adverse reactions / side effects: Hepatic Function Abnormal, Diarrhoea, Sepsis, Dehydration, Gastrointestinal Inflammation, Circulatory Collapse, Bronchitis

Adverse event resulted in: death, hospitalization

Suspect drug(s):
Eloxatin
    Indication: Gastric Cancer
    Start date: 2007-08-01
    End date: 2007-08-01

Fluorouracil
    Indication: Gastric Cancer
    Start date: 2007-08-01
    End date: 2007-08-01

Folinic Acid
    Indication: Gastric Cancer
    Start date: 2007-08-01
    End date: 2007-08-01

Other drugs received by patient: Fumaderm; Novalgin; Nexium



Adverse event in 59 year old female receiving Fluorouracil

Reported by a physician from Germany on 2007-10-25

Patient: 59 year old female

Adverse reactions / side effects: Deafness

Suspect drug(s):
Camptosar
    Dosage: text:6-8 weeks
    Indication: Small Intestine Carcinoma

Fluorouracil
    Dosage: text:6-8 weeks
    Indication: Small Intestine Carcinoma

Folinic Acid
    Dosage: text:6-8 weeks
    Indication: Small Intestine Carcinoma



Adverse event in 65 year old female receiving Fluorouracil

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

Patient: 65 year old female

Adverse reactions / side effects: Sudden Death

Adverse event resulted in: death

Suspect drug(s):
Eloxatin
    Dosage: unk
    Indication: Colon Cancer Metastatic
    Start date: 2007-10-10
    End date: 2007-10-10

Fluorouracil
    Dosage: unk
    Indication: Colon Cancer Metastatic

Leucovorin
    Dosage: unk
    Indication: Colon Cancer Metastatic
    Start date: 2007-10-10
    End date: 2007-10-10

Other drugs received by patient: Anzemet; Decadron



Adverse event in male receiving Fluorouracil

Reported by a individual with unspecified qualification from United States on 2007-10-25

Patient: male, weighing 73.4 kg (161.5 pounds)

Adverse reactions / side effects: Myocardial Ischaemia, Disease Progression, Liver Disorder, Drug Toxicity, Fatigue, Diarrhoea, Myocardial Infarction, Feeling Abnormal

Suspect drug(s):
Bevacizumab (Rhumab Vegf)
    Dosage: 1411 mg
    End date: 2007-09-04

Camptosar
    Dosage: 707 mg
    End date: 2007-09-04

Fluorouracil
    Dosage: 9615 mg
    End date: 2007-09-04

Leucovorin Calcium
    Dosage: 2828 mg
    End date: 2007-09-04



Adverse event in male receiving Fluorouracil

Reported by a individual with unspecified qualification from United States on 2007-10-25

Patient: male, weighing 105.9 kg (233.0 pounds)

Adverse reactions / side effects: Pulmonary Embolism

Suspect drug(s):
Bevacizumab (Rhumab Vegf)
    Dosage: 2100 mg
    End date: 2007-10-15

Camptosar
    Dosage: 1360 mg
    End date: 2007-10-15

Fluorouracil
    Dosage: 20000 mg
    End date: 2007-10-17

Leucovorin Calcium
    Dosage: 3640 mg
    End date: 2007-10-15



Adverse event in female receiving Fluorouracil

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

Patient: female, weighing 137.8 kg (303.2 pounds)

Adverse reactions / side effects: Abdominal Pain, Vomiting, Pyrexia

Adverse event resulted in: hospitalization

Suspect drug(s):
Bevacizumab
    Dosage: 312.5 mg, q2w
    Indication: Colon Cancer
    Start date: 2007-04-23

Fluorouracil
    Dosage: 660 mg, q2w
    Indication: Colon Cancer
    Start date: 2007-04-23

Leucovorin
    Dosage: 660 mg, q2w
    Indication: Colon Cancer
    Start date: 2007-04-23

Oxaliplatin
    Dosage: 140 mg, q2w
    Indication: Colon Cancer
    Start date: 2007-04-23

Other drugs received by patient: Neupogen; Modulon; Iron Supplement



Adverse event in female receiving Fluorouracil

Reported by a individual with unspecified qualification from United States on 2007-10-24

Patient: female, weighing 54.0 kg (118.8 pounds)

Adverse reactions / side effects: Febrile Neutropenia

Adverse event resulted in: hospitalization

Suspect drug(s):
Cisplatin
    Dosage: 68 mg

Ellence
    Dosage: 42 mg

Erbitux
    Dosage: 1125 mg

Fluorouracil
    Dosage: 6300 mg



Adverse event in female receiving Fluorouracil

Reported by a consumer/non-health professional from Australia on 2007-10-24

Patient: female

Adverse reactions / side effects: Osteonecrosis

Suspect drug(s):
Blinded Bevacizumab
    Dosage: unk, q3w
    Indication: Breast Cancer Metastatic
    Start date: 2006-12-21
    End date: 2007-09-04

Blinded Capecitabine
    Dosage: unk, q3w
    Indication: Breast Cancer Metastatic
    Start date: 2006-12-21
    End date: 2007-09-04

Blinded Docetaxel
    Dosage: unk, q3w
    Indication: Breast Cancer Metastatic
    Start date: 2006-12-21
    End date: 2007-09-04

Blinded NO Study Drug Administered
    Dosage: unk, q3w
    Indication: Breast Cancer Metastatic
    Start date: 2006-12-21
    End date: 2007-09-04

Blinded Paclitaxel
    Dosage: unk, q3w
    Indication: Breast Cancer Metastatic
    Start date: 2006-12-21
    End date: 2007-09-04

Blinded Placebo
    Dosage: unk, q3w
    Indication: Breast Cancer Metastatic
    Start date: 2006-12-21
    End date: 2007-09-04

Capecitabine
    Dosage: 2500 mg, d1-14/q3w
    Indication: Breast Cancer Metastatic
    Start date: 2006-12-21

Cyclophosphamide
    Dosage: unk, q3w
    Indication: Breast Cancer Metastatic
    Start date: 2006-12-21
    End date: 2007-09-04

Doxorubicin HCL
    Dosage: unk, q3w
    Indication: Breast Cancer Metastatic
    Start date: 2006-12-21
    End date: 2007-09-04

Epirubicin
    Dosage: unk, q3w
    Indication: Breast Cancer Metastatic
    Start date: 2006-12-21
    End date: 2007-09-04

Fluorouracil
    Dosage: unk, q3w
    Indication: Breast Cancer Metastatic
    Start date: 2006-12-21
    End date: 2007-09-04

Other drugs received by patient: Zoledronic Acid; Perindopril Erbumine



Adverse event in male receiving Fluorouracil

Reported by a individual with unspecified qualification from United States on 2007-10-24

Patient: male, weighing 27.9 kg (61.4 pounds)

Adverse reactions / side effects: Cholecystitis Acute, Enterobacter Sepsis

Adverse event resulted in: hospitalization

Suspect drug(s):
Fluorouracil
    Indication: Metastatic Neoplasm
    Start date: 2007-08-07
    End date: 2007-08-19

Fluorouracil

Irinotecan HCL
    Indication: Metastatic Neoplasm

Leucovorin
    Indication: Metastatic Neoplasm

Sutent
    Dosage: daily dose:25mg-freq:1 daily
    Administration route: Oral
    Indication: Metastatic Neoplasm
    Start date: 2007-08-08
    End date: 2007-08-20



Adverse event in male receiving Fluorouracil

Reported by a individual with unspecified qualification from United States on 2007-10-24

Patient: male, weighing 69.1 kg (152.0 pounds)

Adverse reactions / side effects: Fatigue, Vomiting, Nausea, Proctalgia

Adverse event resulted in: hospitalization

Suspect drug(s):
Bevacizumab (Rhumab Vegf)
    Dosage: 1130 mg
    End date: 2007-09-11

Eloxatin
    Dosage: 479 mg
    End date: 2007-09-11

Fluorouracil
    Dosage: 12632 mg
    End date: 2007-09-11

Leucovorin Calcium
    Dosage: 2256 mg
    End date: 2007-09-11



Adverse event in female receiving Fluorouracil

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

Patient: female

Adverse reactions / side effects: Asthenia

Adverse event resulted in: hospitalization

Suspect drug(s):
Fluorouracil

Irinotecan HCL

Leucovorin

Panitumumab
    Indication: Colorectal Cancer
    Start date: 2007-07-26

Panitumumab
    Start date: 2007-08-14
    End date: 2007-08-14

Other drugs received by patient: Synthroid; Wellbutrin



Adverse event in male receiving Fluorouracil

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):
Aranesp
    Indication: Anaemia

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

Avastin
    Dosage: unk

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

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