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Arixtra (Fondaparinux Subcutaneous) - Disability - Suspected Cause - Side Effect Reports

 
 



Index of reports > Disability (25)

Below is the selection of side effect reports (a.k.a. adverse event reports) related to Arixtra (Fondaparinux Subcutaneous) disability. The selected reports were submitted to the FDA during the sample period of about a year.

Possible Arixtra side effects in male

Reported by a physician from France on 2012-08-24

Patient: male

Reactions: Incorrect Drug Administration Duration, Hemiplegia, Cerebral Haematoma

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Arixtra

Other drugs received by patient: Firmagon; Bisoprolol Fumarate; Nexium; Amlodipine Besylate; Atacand; Lasix; Atorvastatin



Possible Arixtra side effects in male

Reported by a physician from France on 2012-08-21

Patient: male, weighing 87.0 kg (191.4 pounds)

Reactions: Intestinal Ischaemia, Dissociative Disorder, Colitis Ischaemic, Anaemia, Intestinal Obstruction, Delirium, Hypokalaemia, Lung Disorder, Hypomagnesaemia, Hypoalbuminaemia, Suicide Attempt, Septic Shock

Adverse event resulted in: life threatening event, hospitalization, disablity

Drug(s) suspected as cause:
Arixtra
    Start date: 2012-01-01
    End date: 2012-03-01

Atarax

Clozapine
    Dosage: 300 mg to 400 mg per day
    Administration route: Oral
    Indication: Schizophrenia
    Start date: 2012-01-12
    End date: 2012-01-19

Codeine Sulfate
    Administration route: Oral
    Start date: 2012-02-01
    End date: 2012-03-01

Imodium
    Administration route: Oral
    Indication: Diarrhoea
    Start date: 2012-02-01
    End date: 2012-03-01

Nexium
    Administration route: Oral

Sandostatin
    Start date: 2012-02-01
    End date: 2012-03-01

Seroquel
    Dosage: dose progressively increased
    Administration route: Oral
    Indication: Schizophrenia
    Start date: 2012-02-06
    End date: 2012-03-05

Tranxene
    Administration route: Oral
    Indication: Agitation
    Start date: 2012-01-27
    End date: 2012-03-05

Tranxene
    Administration route: Oral
    Indication: Anxiety
    Start date: 2012-01-27
    End date: 2012-03-05



Possible Arixtra side effects in 70 year old male

Reported by a consumer/non-health professional from United States on 2012-08-20

Patient: 70 year old male

Reactions: Malaise, Lung Neoplasm Malignant, Failure To Thrive

Adverse event resulted in: death, disablity

Drug(s) suspected as cause:
Arixtra

Other drugs received by patient: Zofran; Invanz; Topotecan Hydrochloride



Possible Arixtra side effects in male

Reported by a physician from France on 2012-08-17

Patient: male, weighing 87.0 kg (191.4 pounds)

Reactions: Colitis Ischaemic, Intestinal Ischaemia, Dissociative Disorder, Anaemia, Intestinal Obstruction, Delirium, Hypokalaemia, Lung Disorder, Hypomagnesaemia, Hypoalbuminaemia, Suicide Attempt, Septic Shock

Adverse event resulted in: life threatening event, hospitalization, disablity

Drug(s) suspected as cause:
Arixtra
    Start date: 2012-01-01
    End date: 2012-03-01

Atarax

Clozapine
    Dosage: 300 mg to 400 mg per day
    Administration route: Oral
    Indication: Schizophrenia
    Start date: 2012-01-12
    End date: 2012-01-19

Codeine Sulfate
    Administration route: Oral
    Start date: 2012-02-01
    End date: 2012-03-01

Imodium
    Administration route: Oral
    Indication: Diarrhoea
    Start date: 2012-02-01
    End date: 2012-03-01

Nexium
    Administration route: Oral

Sandostatin
    Start date: 2012-02-01
    End date: 2012-03-01

Seroquel
    Dosage: dose progressively increased
    Administration route: Oral
    Indication: Schizophrenia
    Start date: 2012-02-06
    End date: 2012-03-05

Tranxene
    Administration route: Oral
    Indication: Agitation
    Start date: 2012-01-27
    End date: 2012-03-05

Tranxene
    Administration route: Oral
    Indication: Anxiety
    Start date: 2012-01-27
    End date: 2012-03-05



Possible Arixtra side effects in male

Reported by a consumer/non-health professional from France on 2012-06-08

Patient: male

Reactions: Off Label Use, Mydriasis, Subdural Haematoma, Coma, Hemiparesis, Headache, Cerebral Haemorrhage

Adverse event resulted in: life threatening event, hospitalization, disablity

Drug(s) suspected as cause:
Arixtra
    Dosage: 2.5mg per day
    Indication: Thrombosis Prophylaxis
    Start date: 2009-07-21
    End date: 2009-07-22

Lovenox
    Dosage: .4ml per day
    Indication: Thrombosis Prophylaxis
    Start date: 2009-07-18
    End date: 2009-07-20



Possible Arixtra side effects in female

Reported by a physician from Japan on 2012-06-08

Patient: female, weighing 61.0 kg (134.2 pounds)

Reactions: Haemoglobin Decreased, Sciatic Nerve Palsy, Haematocrit Decreased, RED Blood Cell Count Decreased, Incision Site Haematoma, Protein Total Decreased

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Arixtra

Other drugs received by patient: Lipidil; Solon; Amlodipine; Uralyt; Lobu; Urinorm



Possible Arixtra side effects in 51 year old male

Reported by a consumer/non-health professional from United States on 2012-05-16

Patient: 51 year old male

Reactions: Neoplasm Malignant

Adverse event resulted in: death, hospitalization, disablity

Drug(s) suspected as cause:
Arixtra



Possible Arixtra side effects in female

Reported by a health professional (non-physician/pharmacist) from United States on 2012-05-03

Patient: female

Reactions: Death, Multi-Organ Failure, Renal Failure, Heparin-Induced Thrombocytopenia, Pain, Condition Aggravated, Cerebrovascular Accident, Deep Vein Thrombosis

Adverse event resulted in: death, life threatening event, hospitalization, disablity

Drug(s) suspected as cause:
Arixtra

Other drugs received by patient: Unknown



Possible Arixtra side effects in 64 year old male

Reported by a health professional (non-physician/pharmacist) from Ukraine on 2012-04-18

Patient: 64 year old male

Reactions: Dyspnoea, Hyperthermia, Hypotension, Anaphylactoid Reaction

Adverse event resulted in: life threatening event, hospitalization, disablity

Drug(s) suspected as cause:
Arixtra



Possible Arixtra side effects in 74 year old male

Reported by a physician from France on 2012-04-09

Patient: 74 year old male, weighing 79.0 kg (173.8 pounds)

Reactions: Off Label Use, Incorrect Drug Administration Duration, Haematoma

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Arixtra

Other drugs received by patient: Atorvastatin; Furosemide; Acetaminophen and Tramadol HCL; Omeprazole; Bisoprolol Fumarate; Acetaminophen and Codeine Phosphate



Possible Arixtra side effects in female

Reported by a physician from Japan on 2012-04-05

Patient: female, weighing 51.0 kg (112.2 pounds)

Reactions: Cholecystitis Acute

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Arixtra



Possible Arixtra side effects in 51 year old male

Reported by a consumer/non-health professional from United States on 2012-03-13

Patient: 51 year old male

Reactions: Death

Adverse event resulted in: death, hospitalization, disablity

Drug(s) suspected as cause:
Arixtra



Possible Arixtra side effects in 42 year old female

Reported by a health professional (non-physician/pharmacist) from Greece on 2012-03-12

Patient: 42 year old female

Reactions: Paralysis, Extradural Haematoma

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Arixtra

Other drugs received by patient: Epidural



Possible Arixtra side effects in female

Reported by a physician from France on 2012-03-09

Patient: female

Reactions: Muscle Haemorrhage, Off Label Use, Incorrect Drug Administration Duration, Anaemia, Walking Disability

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Arixtra

Other drugs received by patient: Bisoprolol Fumarate; Pantoprazole; Furosemide; Zolpidem



Possible Arixtra side effects in 64 year old male

Reported by a physician from Ukraine on 2012-03-07

Patient: 64 year old male

Reactions: Dyspnoea, Hyperthermia, Hypotension, Anaphylactoid Reaction

Adverse event resulted in: life threatening event, disablity

Drug(s) suspected as cause:
Arixtra



Possible Arixtra side effects in male

Reported by a physician from Japan on 2012-03-06

Patient: male, weighing 3.2 kg (7.0 pounds)

Reactions: Congenital Cleft Hand, Syndactyly, Maternal Drugs Affecting Foetus, Foetal Exposure During Pregnancy, Adactyly, Haemangioma Congenital

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Arixtra
    Dosage: 7.5mg per day
    Indication: Thrombosis Prophylaxis
    Start date: 2011-05-24
    End date: 2011-06-03

Arixtra
    Dosage: 5mg per day
    Start date: 2011-06-04
    End date: 2011-12-28



Possible Arixtra side effects in female

Reported by a physician from Japan on 2012-02-23

Patient: female, weighing 51.0 kg (112.2 pounds)

Reactions: Cholecystitis Acute

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Arixtra



Possible Arixtra side effects in

Reported by a physician from Japan on 2012-02-21

Patient:

Reactions: Syndactyly, Birth Mark, Foetal Exposure During Pregnancy, Adactyly

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Arixtra



Possible Arixtra side effects in 37 year old female

Reported by a pharmacist from United States on 2012-02-03

Patient: 37 year old female

Reactions: Heparin-Induced Thrombocytopenia

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Arixtra

Other drugs received by patient: Lamictal; Tracleer



Possible Arixtra side effects in 66 year old female

Reported by a pharmacist from United States on 2011-12-19

Patient: 66 year old female, weighing 102.0 kg (224.4 pounds)

Reactions: Renal Impairment, Hypotension, Blood Creatinine Increased, Retroperitoneal Haemorrhage, International Normalised Ratio Fluctuation

Adverse event resulted in: life threatening event, hospitalization, disablity

Drug(s) suspected as cause:
Arixtra
    Dosage: arixtra injection
    Indication: Deep Vein Thrombosis
    Start date: 2011-10-24
    End date: 2011-10-31

Coumadin

Other drugs received by patient: Zocor; Celebrex; Buspar; Percocet; Protonix; Metformin HCL; Vitamin D; Claritin; Lexapro; Potassium Chloride; Benefiber; Levothyroxine Sodium



Possible Arixtra side effects in female

Reported by a health professional (non-physician/pharmacist) from France on 2011-12-06

Patient: female, weighing 66.0 kg (145.2 pounds)

Reactions: Incorrect Drug Administration Duration, Intraventricular Haemorrhage, Coma

Adverse event resulted in: life threatening event, hospitalization, disablity

Drug(s) suspected as cause:
Arixtra

Other drugs received by patient: Doxorubicin Hydrochloride; Heparin; Aromasin



Possible Arixtra side effects in 73 year old female

Reported by a health professional (non-physician/pharmacist) from United States on 2011-11-30

Patient: 73 year old female

Reactions: Death, Hospitalisation

Adverse event resulted in: death, life threatening event, hospitalization, disablity

Drug(s) suspected as cause:
Arixtra

Other drugs received by patient: Antibiotic



Possible Arixtra side effects in 66 year old female

Reported by a consumer/non-health professional from United States on 2011-11-11

Patient: 66 year old female, weighing 102.0 kg (224.4 pounds)

Reactions: Renal Impairment, Prothrombin Time Abnormal, Hypotension, Blood Creatinine Increased, Retroperitoneal Haemorrhage, International Normalised Ratio Fluctuation

Adverse event resulted in: life threatening event, hospitalization, disablity

Drug(s) suspected as cause:
Arixtra
    Dosage: 10mg per day
    Indication: Deep Vein Thrombosis
    Start date: 2011-10-24
    End date: 2011-10-31

Coumadin
    Indication: Product Used FOR Unknown Indication

Other drugs received by patient: Claritin; Metformin HCL; Celebrex; Percocet; Levothyroxine Sodium; Benefiber; Zocor; Protonix; Vitamin D; Lexapro; Buspar; Potassium



Possible Arixtra side effects in female

Reported by a health professional (non-physician/pharmacist) from France on 2011-10-27

Patient: female, weighing 60.0 kg (132.0 pounds)

Reactions: Incorrect Drug Administration Duration, Intraventricular Haemorrhage, Coma

Adverse event resulted in: life threatening event, hospitalization, disablity

Drug(s) suspected as cause:
Arixtra

Other drugs received by patient: Doxorubicin Hydrochloride; Heparin



Possible Arixtra side effects in female

Reported by a physician from France on 2011-10-06

Patient: female, weighing 62.0 kg (136.4 pounds)

Reactions: Pain, Petechiae, Underdose, Multifocal Motor Neuropathy, Hypoaesthesia, Paraesthesia, Off Label Use, Incorrect Drug Administration Duration, Neuropathy Peripheral, Oedema Peripheral

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Arixtra
    Dosage: 2.5mg per day
    Indication: Thrombosis Prophylaxis
    Start date: 2011-03-11
    End date: 2011-04-11

Arixtra
    Dosage: 5mg per day
    Indication: Deep Vein Thrombosis
    Start date: 2011-01-01
    End date: 2011-03-01

Other drugs received by patient: TED Stockings

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