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Arixtra Side Effects Report #5647007-4
Consumer or non-health professional from FRANCE reported ARIXTRA problem on Feb 20, 2008. Female patient, 46 years of age, was diagnosed with deep vein thrombosis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: haemarthrosis, haemorrhagic anaemia, incorrect dose administered, joint swelling, muscle haemorrhage, overdose, pain in extremity, . ARIXTRA dosage: 15MG PER DAY. During the same period patient was treated with BACTRIM, ENALAPRIL MALEATE, CORTANCYL, NEORAL, OMEPRAZOLE, OROCAL D. Patient was hospitalized and became disabled. Patient recovered.

Arixtra Side Effects Report #5663120-X
ARIXTRA problem was reported by a Consumer or non-health professional from FRANCE on Mar 07, 2008. Female patient, 46 years of age, weighting 160.9 lb, was diagnosed with deep vein thrombosis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: haemarthrosis, haemorrhagic anaemia, incorrect dose administered, joint swelling, muscle haemorrhage, overdose, pain in extremity, . ARIXTRA dosage: 15MG PER DAY. During the same period patient was treated with BACTRIM, RENITEC, CORTANCYL, NEORAL, OMEPRAZOLE, OROCAL D. Patient was hospitalized and became disabled. Patient recovered.

Novolog Side Effects Report #5624255-0
Physician from IRAN (ISLAMIC REPUBLIC OF) reported NOVOLOG problem on Feb 02, 2008. Male patient, weighting 239.2 lb, was diagnosed with diabetes mellitus and was treated with NOVOLOG. After drug was administered, patient experienced the following problems/side effects: haemarthrosis, . NOVOLOG dosage: unknown. During the same period patient was treated with METFORMIN. Patient was hospitalized. Patient recovered.

Novolog Side Effects Report #5632895-8
NOVOLOG problem was reported by a Physician from IRAN (ISLAMIC REPUBLIC OF) on Feb 12, 2008. Male patient, weighting 239.2 lb, was diagnosed with diabetes mellitus and was treated with NOVOLOG. After drug was administered, patient experienced the following problems/side effects: haemarthrosis, . NOVOLOG dosage: unknown. During the same period patient was treated with METFORMIN. Patient was hospitalized. Patient recovered.


Arixtra Side Effects Report #5584271-4
Consumer or non-health professional from FRANCE reported ARIXTRA problem on Dec 31, 2007. Male patient, 31 years of age, weighting 165.3 lb, was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: haemarthrosis, . ARIXTRA dosage: 2.5MG PER DAY. Patient was hospitalized. Patient recovered.

Aptivus Side Effects Report #5585082-6
APTIVUS problem was reported by a Consumer or non-health professional from on Jan 02, 2008. Male patient, 31 years of age, was diagnosed with hiv infection and was treated with APTIVUS. After drug was administered, patient experienced the following problems/side effects: haemarthrosis, haemorrhagic diathesis, soft tissue haemorrhage, . APTIVUS dosage: TIPRANAVIR 1000 MG/RITONAVIR 400 MG. Patient recovered.

Aptivus Side Effects Report #5585088-7
Consumer or non-health professional from reported APTIVUS problem on Jan 02, 2008. Male patient, 27 years of age, was diagnosed with hiv infection and was treated with APTIVUS. After drug was administered, patient experienced the following problems/side effects: haemarthrosis, haemorrhagic diathesis, injection site bruising, injection site haematoma, soft tissue haemorrhage, . APTIVUS dosage: TIPRANAVIR 1000 MG/RITONAVIR 400 MG. During the same period patient was treated with FUZEON. Patient recovered.

Aptivus Side Effects Report #5585948-7
APTIVUS problem was reported by a Consumer or non-health professional from on Jan 02, 2008. Male patient, 27 years of age, was diagnosed with hiv infection and was treated with APTIVUS. After drug was administered, patient experienced the following problems/side effects: haemarthrosis, haemorrhagic diathesis, injection site bruising, injection site haematoma, soft tissue haemorrhage, . APTIVUS dosage: TIPRANAVIR 1000 MG/RITONAVIR 400 MG. During the same period patient was treated with FUZEON. Patient recovered.

Advate Side Effects Report #5514684-8
Consumer or non-health professional from UNITED STATES reported ADVATE problem on Nov 02, 2007. Male patient, child 6 years of age, was diagnosed with prophylaxis and was treated with ADVATE. After drug was administered, patient experienced the following problems/side effects: haemarthrosis, . ADVATE dosage: unknown. Patient recovered.


Arixtra Side Effects Report #5483591-1
ARIXTRA problem was reported by a Pharmacist from UNITED STATES on Oct 10, 2007. Male patient, 62 years of age, weighting 233.7 lb, was diagnosed with thrombosis prophylaxis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: haemarthrosis, platelet count decreased, . ARIXTRA dosage: 2.5MG DAILY SUBC.. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5483802-2
Consumer or non-health professional from FRANCE reported ARIXTRA problem on Oct 03, 2007. Male patient, 31 years of age, weighting 165.3 lb, was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: haemarthrosis, . ARIXTRA dosage: 2.5MG PER DAY. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5470984-1
ARIXTRA problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 24, 2007. Male patient, 64 years of age, was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: haemarthrosis, incision site haematoma, joint effusion, . ARIXTRA dosage: 2.5MG PER DAY. During the same period patient was treated with SIMVASTATIN. Patient recovered.

Advate Side Effects Report #5411101-3
Consumer or non-health professional from UNITED STATES reported ADVATE problem on Dec 01, 2006. Male patient, 45 years of age, was diagnosed with factor viii deficiency and was treated with ADVATE. After drug was administered, patient experienced the following problems/side effects: haemarthrosis, skin disorder, . ADVATE dosage: unknown. During the same period patient was treated with DILAUDID, CELEBREX, VALIUM, ICY HOT, TRAUMEEL AND PO SUM ON LINEMENT. Patient recovered.

Humira Side Effects Report #5401008-X
HUMIRA problem was reported by a Health Professional from UNITED KINGDOM on July 20, 2007. Male patient, weighting 134.3 lb, was diagnosed with rheumatoid arthritis, analgesia and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: haemarthrosis, pain, swelling, . HUMIRA dosage: unknown. During the same period patient was treated with PARACETAMOL, IBUPROFEN, METHOTREXATE, BRUFEN RETARD. Patient was hospitalized and became disabled. Patient recovered.


Humira Side Effects Report #5401027-3
Health Professional from UNITED KINGDOM reported HUMIRA problem on July 20, 2007. Male patient, weighting 134.3 lb, was diagnosed with rheumatoid arthritis, analgesia and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: haemarthrosis, meniscus lesion, pain, swelling, . HUMIRA dosage: unknown. During the same period patient was treated with IBUPROFEN, PARACETAMOL, METHOTREXATE. Patient was hospitalized and became disabled. Patient recovered.

Humira Side Effects Report #5401008-X
HUMIRA problem was reported by a Health Professional from UNITED KINGDOM on July 20, 2007. Male patient, weighting 134.3 lb, was diagnosed with rheumatoid arthritis, analgesia and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: haemarthrosis, pain, swelling, . HUMIRA dosage: unknown. During the same period patient was treated with PARACETAMOL, IBUPROFEN, METHOTREXATE, BRUFEN RETARD. Patient was hospitalized and became disabled. Patient recovered.

Humira Side Effects Report #5401027-3
Health Professional from UNITED KINGDOM reported HUMIRA problem on July 20, 2007. Male patient, weighting 134.3 lb, was diagnosed with rheumatoid arthritis, analgesia and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: haemarthrosis, meniscus lesion, pain, swelling, . HUMIRA dosage: unknown. During the same period patient was treated with IBUPROFEN, PARACETAMOL, METHOTREXATE. Patient was hospitalized and became disabled. Patient recovered.

Truvada Side Effects Report #5711947-8
TRUVADA problem was reported by a Physician from FRANCE on Apr 09, 2008. Male patient, 36 years of age, was diagnosed with hiv infection and was treated with TRUVADA. After drug was administered, patient experienced the following problems/side effects: haemarthrosis, hypertension, osteopenia, . TRUVADA dosage: unknown. During the same period patient was treated with EFAVIRENZ. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5344100-0
Physician from FRANCE reported ARIXTRA problem on June 01, 2007. Male patient, 73 years of age, weighting 201.7 lb, was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: haemarthrosis, . ARIXTRA dosage: 2.5MG PER DAY. During the same period patient was treated with DIAMICRON, ALLOPURINOL, ACETAMINOPHEN, TOPALGIC. Patient was hospitalized. Patient recovered.


Humira Side Effects Report #5346224-0
HUMIRA problem was reported by a Health Professional from UNITED KINGDOM on May 28, 2007. Male patient, weighting 134.3 lb, was diagnosed with rheumatoid arthritis, analgesic effect and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: haemarthrosis, pain, swelling, . HUMIRA dosage: unknown. During the same period patient was treated with PARACETAMOL, IBUPROFEN, METHOTREXATE, BRUFEN RETARD. Patient was hospitalized and became disabled. Patient recovered.

Vyvanse Side Effects Report #5660001-2
Consumer or non-health professional from UNITED STATES reported VYVANSE problem on Feb 22, 2008. Male patient, 13 years of age, weighting 130.1 lb, was diagnosed with attention deficit/hyperactivity disorder and was treated with VYVANSE. After drug was administered, patient experienced the following problems/side effects: contusion, haemarthrosis, off label use, . VYVANSE dosage: 50 MG, 1X/DAY; QE, ORAL. During the same period patient was treated with HELIXATE, ACETAMINOPHEN. Patient recovered.

Humira Side Effects Report #5667710-X
HUMIRA problem was reported by a Physician from UNITED STATES on Jan 15, 2008. Male patient, 40 years of age, was diagnosed with psoriatic arthropathy and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: ecchymosis, haemarthrosis, . HUMIRA dosage: unknown. During the same period patient was treated with PREDNISONE. Patient recovered.

Novolog Side Effects Report #5612195-2
Physician from IRAN (ISLAMIC REPUBLIC OF) reported NOVOLOG problem on Jan 22, 2008. Male patient, weighting 239.2 lb, was diagnosed with diabetes mellitus and was treated with NOVOLOG. After drug was administered, patient experienced the following problems/side effects: fall, haemarthrosis, post procedural complication, . NOVOLOG dosage: unknown. During the same period patient was treated with METFORMIN. Patient was hospitalized. Patient recovered.

Fuzeon Side Effects Report #5612481-6
FUZEON problem was reported by a Health Professional from UNITED KINGDOM on Jan 21, 2008. Male patient, 27 years of age, was treated with FUZEON. After drug was administered, patient experienced the following problems/side effects: contusion, haemarthrosis, haematoma, soft tissue haemorrhage, . FUZEON dosage: unknown. During the same period patient was treated with TIPRANAVIR, RITONAVIR. Patient recovered.

Fuzeon Side Effects Report #5612500-7
Health Professional from UNITED KINGDOM reported FUZEON problem on Jan 21, 2008. Male patient, 30 years of age, was treated with FUZEON. After drug was administered, patient experienced the following problems/side effects: contusion, haemarthrosis, haematoma, soft tissue haemorrhage, . FUZEON dosage: unknown. During the same period patient was treated with TIPRANAVIR, RITONAVIR. Patient recovered.

Benefix Side Effects Report #5621623-8
BENEFIX problem was reported by a Physician from UNITED KINGDOM on Feb 01, 2008. Male patient was diagnosed with factor ix deficiency and was treated with BENEFIX. After drug was administered, patient experienced the following problems/side effects: epistaxis, haemarthrosis, pyrexia, . BENEFIX dosage: unknown. Patient was hospitalized. Patient recovered.

Clamoxyl Side Effects Report #5588785-2
Consumer or non-health professional from FRANCE reported CLAMOXYL problem on Jan 09, 2008. Male patient, 83 years of age, was diagnosed with thrombosis prophylaxis and was treated with CLAMOXYL. After drug was administered, patient experienced the following problems/side effects: epistaxis, haemarthrosis, staphylococcal infection, . CLAMOXYL dosage: unknown. During the same period patient was treated with ZYLORIC, PREVISCAN, PERSANTINE, ZOCOR, STILNOX, MEPRONIZINE, APROVEL, LASILIX. Patient was hospitalized. Patient recovered.

Zocor Side Effects Report #5588981-4
ZOCOR problem was reported by a Health Professional from FRANCE on Jan 09, 2008. Male patient, 83 years of age, was diagnosed with atrial fibrillation, endocarditis and was treated with ZOCOR. After drug was administered, patient experienced the following problems/side effects: epistaxis, haemarthrosis, . ZOCOR dosage: unknown. During the same period patient was treated with FLUINDIONE, DIPYRIDAMOLE, ALLOPURINOL, AMOXICILLIN, ZOLPIDEM TARTRATE. Patient was hospitalized. Patient recovered.

Benefix Side Effects Report #5602795-8
Health Professional from UNITED STATES reported BENEFIX problem on Jan 15, 2008. Male patient, weighting 79.81 lb, was treated with BENEFIX. After drug was administered, patient experienced the following problems/side effects: haemarthrosis, mouth haemorrhage, . BENEFIX dosage: unknown. Patient recovered.

Cystagon Side Effects Report #5572338-6
CYSTAGON problem was reported by a Physician from FRANCE on Dec 10, 2007. Male patient, child 8 years of age, was diagnosed with cystinosis and was treated with CYSTAGON. After drug was administered, patient experienced the following problems/side effects: angiopathy, haemarthrosis, scar, subcutaneous abscess, . CYSTAGON dosage: ; DAILY; ORAL, 10 MG/KG; 4 TIMES A DAY; ORAL. During the same period patient was treated with ALPHACALCIDOL, INDOCID. Patient recovered.

Refacto Side Effects Report #5488049-1
Health Professional from FRANCE reported REFACTO problem on Oct 15, 2007. Male patient, weighting 160.9 lb, was diagnosed with factor viii deficiency and was treated with REFACTO. After drug was administered, patient experienced the following problems/side effects: anti factor viii antibody positive, haemarthrosis, haematoma, . REFACTO dosage: unknown. Patient recovered.

Benefix Side Effects Report #5428918-1
BENEFIX problem was reported by a Physician from NETHERLANDS on Aug 21, 2007. Male patient, weighting 33.07 lb, was diagnosed with factor ix deficiency and was treated with BENEFIX. After drug was administered, patient experienced the following problems/side effects: haemarthrosis, . BENEFIX dosage: unknown. Patient recovered.

Benefix Side Effects Report #5398945-1
Physician from UNITED KINGDOM reported BENEFIX problem on July 19, 2007. Male patient was diagnosed with factor ix deficiency and was treated with BENEFIX. After drug was administered, patient experienced the following problems/side effects: epistaxis, haemarthrosis, pyrexia, . BENEFIX dosage: unknown. Patient was hospitalized. Patient recovered.

Benefix Side Effects Report #5398945-1
BENEFIX problem was reported by a Physician from UNITED KINGDOM on July 19, 2007. Male patient was diagnosed with factor ix deficiency and was treated with BENEFIX. After drug was administered, patient experienced the following problems/side effects: epistaxis, haemarthrosis, pyrexia, . BENEFIX dosage: unknown. Patient was hospitalized. Patient recovered.

Fuzeon Side Effects Report #5766534-2
Health Professional from UNITED KINGDOM reported FUZEON problem on May 30, 2008. Male patient, 27 years of age, was treated with FUZEON. After drug was administered, patient experienced the following problems/side effects: contusion, haemarthrosis, haematoma, haemorrhagic diathesis, soft tissue haemorrhage, . FUZEON dosage: unknown. During the same period patient was treated with TIPRANAVIR, RITONAVIR. Patient recovered.

Benefix Side Effects Report #5774548-1
BENEFIX problem was reported by a Health Professional from AUSTRALIA on June 12, 2008. Male patient, weighting 165.3 lb, was diagnosed with factor ix deficiency and was treated with BENEFIX. After drug was administered, patient experienced the following problems/side effects: haemarthrosis, haemorrhage, . BENEFIX dosage: unknown. Patient recovered.

Benefix Side Effects Report #5786304-9
Health Professional from UNITED STATES reported BENEFIX problem on June 16, 2008. Male patient, weighting 79.81 lb, was diagnosed with haemophilia and was treated with BENEFIX. After drug was administered, patient experienced the following problems/side effects: haemarthrosis, mouth haemorrhage, . BENEFIX dosage: unknown. Patient recovered.

Benefix Side Effects Report #5788038-3
BENEFIX problem was reported by a Health Professional from AUSTRALIA on June 12, 2008. Male patient, weighting 123.0 lb, was diagnosed with factor ix deficiency and was treated with BENEFIX. After drug was administered, patient experienced the following problems/side effects: haemarthrosis, haemorrhage, . BENEFIX dosage: unknown. Patient recovered.

Benefix Side Effects Report #5793703-8
Health Professional from AUSTRALIA reported BENEFIX problem on June 17, 2008. Male patient, weighting 165.3 lb, was diagnosed with factor ix deficiency and was treated with BENEFIX. After drug was administered, patient experienced the following problems/side effects: haemarthrosis, haemorrhage, . BENEFIX dosage: unknown. Patient recovered.

Benefix Side Effects Report #5793791-9
BENEFIX problem was reported by a Health Professional from AUSTRALIA on June 17, 2008. Male patient, weighting 123.0 lb, was diagnosed with factor ix deficiency and was treated with BENEFIX. After drug was administered, patient experienced the following problems/side effects: haemarthrosis, haemorrhage, . BENEFIX dosage: unknown. Patient recovered.

Benefix Side Effects Report #5740827-7
Health Professional from AUSTRALIA reported BENEFIX problem on May 08, 2008. Male patient, weighting 123.0 lb, was diagnosed with factor ix deficiency and was treated with BENEFIX. After drug was administered, patient experienced the following problems/side effects: haemarthrosis, haemorrhage, . BENEFIX dosage: unknown. Patient recovered.

Benefix Side Effects Report #5740828-9
BENEFIX problem was reported by a Health Professional from AUSTRALIA on May 08, 2008. Male patient, weighting 165.3 lb, was diagnosed with factor ix deficiency and was treated with BENEFIX. After drug was administered, patient experienced the following problems/side effects: haemarthrosis, haemorrhage, . BENEFIX dosage: unknown. Patient recovered.

Thalomid Side Effects Report #5748601-2
Consumer or non-health professional from UNITED STATES reported THALOMID problem on May 09, 2008. Male patient, 66 years of age, was diagnosed with multiple myeloma and was treated with THALOMID. After drug was administered, patient experienced the following problems/side effects: blood immunoglobulin a increased, haemarthrosis, haemorrhage, platelet count decreased, splenic haemorrhage, stem cell transplant, white blood cell count decreased, . THALOMID dosage: 200 MG, DAILY, ORAL; 200-400 MG, DAILY, ORAL. During the same period patient was treated with DEXAMETHASONE, AMBIEN, GLUCOSAMINE, VITAMIN, ACETAMINOPHEN. Patient was hospitalized. Patient recovered.

Betamethasone Side Effects Report #5694374-1
BETAMETHASONE DIPROPIONATE problem was reported by a Physician from CHINA on Mar 27, 2008. Male patient, 77 years of age, weighting 176.4 lb, was diagnosed with osteoarthritis and was treated with BETAMETHASONE DIPROPIONATE. After drug was administered, patient experienced the following problems/side effects: ecchymosis, haemarthrosis, . BETAMETHASONE DIPROPIONATE dosage: 1 ML; QD; IA. During the same period patient was treated with HYALURONATE. Patient was hospitalized. Patient recovered.

Benefix Side Effects Report #5712213-7
Physician from NETHERLANDS reported BENEFIX problem on Apr 09, 2008. Male patient, weighting 33.07 lb, was diagnosed with factor ix deficiency and was treated with BENEFIX. After drug was administered, patient experienced the following problems/side effects: haemarthrosis, . BENEFIX dosage: unknown. Patient recovered.

Arixtra Side Effects Report #5355599-8
ARIXTRA problem was reported by a Consumer or non-health professional from UNITED STATES on June 11, 2007. Female patient was diagnosed with prophylaxis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: arthralgia, haemarthrosis, joint swelling, musculoskeletal stiffness, . ARIXTRA dosage: 2.5MG PER DAY. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5360500-7
Physician from FRANCE reported ARIXTRA problem on June 08, 2007. Male patient, 73 years of age, weighting 201.7 lb, was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: activated partial thromboplastin time prolonged, haemarthrosis, platelet count increased, . ARIXTRA dosage: 2.5MG PER DAY. During the same period patient was treated with ALLOPURINOL, ACETAMINOPHEN, TOPALGIC, NEXIUM, RENITEC, DIAMICRON, HEXAQUINE. Patient was hospitalized. Patient recovered.

Aptivus Side Effects Report #5327925-7
APTIVUS problem was reported by a Physician from FRANCE on May 14, 2007. Male patient, 48 years of age, weighting 121.3 lb, was diagnosed with hiv infection and was treated with APTIVUS. After drug was administered, patient experienced the following problems/side effects: coagulation factor decreased, haemarthrosis, . APTIVUS dosage: unknown. During the same period patient was treated with VIREAD, KIVEXA. Patient was hospitalized. Patient recovered.

Aptivus Side Effects Report #5331523-9
Physician from FRANCE reported APTIVUS problem on May 14, 2007. Male patient, 48 years of age, weighting 121.3 lb, was diagnosed with hiv infection and was treated with APTIVUS. After drug was administered, patient experienced the following problems/side effects: coagulation factor decreased, haemarthrosis, . APTIVUS dosage: TPV/RTV COADM. RTV: 400 MG. During the same period patient was treated with VIREAD, KIVEXA. Patient was hospitalized. Patient recovered.

Nexium Side Effects Report #5312348-7
NEXIUM problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 16, 2006. Female patient, 73 years of age, weighting 145.1 lb, was diagnosed with gastrooesophageal reflux disease and was treated with NEXIUM. After drug was administered, patient experienced the following problems/side effects: gait disturbance, haemarthrosis, joint stiffness, joint swelling, . NEXIUM dosage: unknown. During the same period patient was treated with FOSAMAX, TOPROL. Patient recovered.

Fenofibrate Side Effects Report #5272572-9
Consumer or non-health professional from FRANCE reported FENOFIBRATE problem on Mar 19, 2007. Female patient, 65 years of age, was diagnosed with dyslipidaemia, atrial fibrillation, mitral valve replacement and was treated with FENOFIBRATE. After drug was administered, patient experienced the following problems/side effects: haemarthrosis, international normalised ratio increased, melaena, normochromic normocytic anaemia, renal failure acute, . FENOFIBRATE dosage: unknown. During the same period patient was treated with WARFARIN. Patient was hospitalized. Patient recovered.