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Triquilar Side Effects Report #5614114-1
Health Professional from JAPAN reported TRIQUILAR problem on Jan 25, 2008. Female patient, 40 years of age, was diagnosed with endometriosis, contraception and was treated with TRIQUILAR. After drug was administered, patient experienced the following problems/side effects: hypercoagulation, thrombophlebitis superficial, . TRIQUILAR dosage: unknown. During the same period patient was treated with KEISHIBUKURYOUGAN. Patient was hospitalized. Patient recovered.

Triquilar Side Effects Report #5615858-8
TRIQUILAR problem was reported by a Health Professional from JAPAN on Jan 25, 2008. Female patient, 40 years of age, was diagnosed with endometriosis, contraception and was treated with TRIQUILAR. After drug was administered, patient experienced the following problems/side effects: hypercoagulation, thrombophlebitis superficial, . TRIQUILAR dosage: unknown. During the same period patient was treated with KEISHIBUKURYOUGAN. Patient was hospitalized. Patient recovered.

Testosterone Side Effects Report #5597974-2
Physician from GERMANY reported TESTOSTERONE problem on Jan 02, 2008. Male patient, 30 years of age, was diagnosed with klinefelter's syndrome and was treated with TESTOSTERONE. After drug was administered, patient experienced the following problems/side effects: hypercoagulation, peripheral arterial occlusive disease, thrombosis, . TESTOSTERONE dosage: unknown. Patient was hospitalized. Patient recovered.

Clolar Side Effects Report #5603615-8
CLOLAR problem was reported by a Physician from UNITED STATES on Jan 14, 2008. Male patient, 15 years of age, weighting 166.4 lb, was diagnosed with myeloid leukaemia and was treated with CLOLAR. After drug was administered, patient experienced the following problems/side effects: hypercoagulation, pulmonary embolism, . CLOLAR dosage: unknown. Patient died on 01/13/2008.


Paracetamol Side Effects Report #5495054-8
Health Professional from GREECE reported PARACETAMOL BP problem on Oct 10, 2007. Female patient was treated with PARACETAMOL BP. After drug was administered, patient experienced the following problems/side effects: hypercoagulation, peripheral ischaemia, . PARACETAMOL BP dosage: 500 MG, UNK. During the same period patient was treated with PHYTOMENADIONE, PIPERACILLIN, TAZOBACTAM, OMEPRAZOLE, CIPROFLOXACIN, CLINDAMYCIN, ENOXAPARIN, FOLIC ACID. Patient was hospitalized. Patient recovered.

Acetaminophen Side Effects Report #5503079-9
ACETAMINOPHEN problem was reported by a Health Professional from GREECE on Oct 17, 2007. Female patient was treated with ACETAMINOPHEN. After drug was administered, patient experienced the following problems/side effects: hypercoagulation, peripheral ischaemia, . ACETAMINOPHEN dosage: 500 MG, UNK. During the same period patient was treated with PHYTOMENADIONE, PIPERACILLIN, TAZOBACTAM, OMEPRAZOLE, CIPROFLOXACIN, CLINDAMYCIN, ENOXAPARIN. Patient was hospitalized. Patient recovered.

Avonex Side Effects Report #5424863-6
Consumer or non-health professional from UNITED STATES reported AVONEX problem on Aug 08, 2007. Female patient, 31 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: hypercoagulation, . AVONEX dosage: unknown. Patient recovered.

Zeldox Side Effects Report #5792433-6
ZELDOX problem was reported by a Physician from GERMANY on June 16, 2008. Female patient, 23 years of age, was diagnosed with borderline personality disorder, schizophrenia and was treated with ZELDOX. After drug was administered, patient experienced the following problems/side effects: hypercoagulation, thrombosis, . ZELDOX dosage: unknown. During the same period patient was treated with FLUPENTIXOL DECANOATE, FLUPENTIXOL DECANOATE, LORAZEPAM, DIAZEPAM. Patient recovered.

Byetta Side Effects Report #5319370-5
Physician from UNITED STATES reported BYETTA problem on May 01, 2007. Male patient, 52 years of age, was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: hypercoagulation, intestinal obstruction, mesenteric artery thrombosis, pulmonary embolism, . BYETTA dosage: unknown. Patient was hospitalized. Patient recovered.


Myozyme Side Effects Report #5292567-9
MYOZYME problem was reported by a Physician from ITALY on Mar 22, 2007. Male patient, 40 years of age, was diagnosed with glycogen storage disease type ii and was treated with MYOZYME. After drug was administered, patient experienced the following problems/side effects: hypercoagulation, pain in extremity, protein s abnormal, venous occlusion, . MYOZYME dosage: 1300 MG Q2WKS IV. Patient recovered.

Omepral Side Effects Report #5312411-0
Physician from JAPAN reported OMEPRAL problem on Apr 26, 2007. Female patient, 79 years of age, was diagnosed with reflux oesophagitis and was treated with OMEPRAL. After drug was administered, patient experienced the following problems/side effects: hypercoagulation, platelet count decreased, . OMEPRAL dosage: unknown. During the same period patient was treated with HEPARIN. Patient recovered.

Celebrex Side Effects Report #5139993-6
CELEBREX problem was reported by a Physician from UNITED STATES on Oct 11, 2006. Female patient, 19 years of age, was diagnosed with oedema peripheral, pain in extremity, psoriatic arthropathy and was treated with CELEBREX. After drug was administered, patient experienced the following problems/side effects: hypercoagulation, post procedural pulmonary embolism, syncope, . CELEBREX dosage: 400 MG (200 MG, 2 IN 1 D). During the same period patient was treated with PREDNISONE, EFFEXOR, PEPCID, METHOTREXATE, FOLIC ACID. Patient recovered.

Myozyme Side Effects Report #5255825-X
Physician from ITALY reported MYOZYME problem on Feb 15, 2007. Male patient, 40 years of age, was diagnosed with glycogen storage disease type ii and was treated with MYOZYME. After drug was administered, patient experienced the following problems/side effects: hypercoagulation, infusion related reaction, pain in extremity, protein s decreased, venous occlusion, . MYOZYME dosage: 1300 MG/KG Q2WKS IV. Patient recovered.

Myozyme Side Effects Report #5268627-5
MYOZYME problem was reported by a Physician from ITALY on Mar 01, 2007. Male patient, 40 years of age, was diagnosed with glycogen storage disease type ii and was treated with MYOZYME. After drug was administered, patient experienced the following problems/side effects: hypercoagulation, pain in extremity, venous occlusion, . MYOZYME dosage: 1300 MG Q2WKS IV. Patient recovered.


Nuvaring Side Effects Report #5542598-6
Pharmacist from UNITED STATES reported NUVARING problem on Dec 05, 2007. Female patient, weighting 151.0 lb, was diagnosed with contraception and was treated with NUVARING. After drug was administered, patient experienced the following problems/side effects: abdominal pain, hypercoagulation, portal vein thrombosis, . NUVARING dosage: unknown. Patient was hospitalized. Patient recovered.

Avonex Side Effects Report #5481911-5
AVONEX problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 20, 2007. Female patient, 31 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: hypercoagulation, umbilical cord abnormality, . AVONEX dosage: unknown. Patient recovered.

Enoxaparin Side Effects Report #5447355-7
Consumer or non-health professional from AUSTRALIA reported ENOXAPARIN problem on Sept 05, 2007. Male patient, 55 years of age, weighting 152.1 lb, was diagnosed with pulmonary embolism and was treated with ENOXAPARIN. After drug was administered, patient experienced the following problems/side effects: chest pain, hypercoagulation, international normalised ratio increased, . ENOXAPARIN dosage: 1 MG/KG BID - SUBCUTANEOUS. During the same period patient was treated with FRUSEMIDE, VENLAFAXIINE, PARACETAMOL, FELODIPINE. Patient was hospitalized. Patient recovered.

Salazopyrin Side Effects Report #5392839-3
SALAZOPYRIN problem was reported by a Consumer or non-health professional from IRELAND on July 09, 2007. Female patient, 34 years of age, was diagnosed with colitis ulcerative and was treated with SALAZOPYRIN. After drug was administered, patient experienced the following problems/side effects: colitis, hypercoagulation, neutrophilia, pain in extremity, . SALAZOPYRIN dosage: unknown. During the same period patient was treated with PREDNISOLONE, HYDROCORTISONE, CYCLOSPORINE. Patient recovered.

Celebrex Side Effects Report #5399488-1
Consumer or non-health professional from UNITED STATES reported CELEBREX problem on July 12, 2007. Male patient, weighting 220.0 lb, was diagnosed with inflammation, limb injury, back injury, pain and was treated with CELEBREX. After drug was administered, patient experienced the following problems/side effects: deep vein thrombosis, hypercoagulation, myocardial infarction, transient ischaemic attack, . CELEBREX dosage: unknown. During the same period patient was treated with BEXTRA, VIOXX. Patient recovered.


Salazopyrin Side Effects Report #5392839-3
SALAZOPYRIN problem was reported by a Consumer or non-health professional from IRELAND on July 09, 2007. Female patient, 34 years of age, was diagnosed with colitis ulcerative and was treated with SALAZOPYRIN. After drug was administered, patient experienced the following problems/side effects: colitis, hypercoagulation, neutrophilia, pain in extremity, . SALAZOPYRIN dosage: unknown. During the same period patient was treated with PREDNISOLONE, HYDROCORTISONE, CYCLOSPORINE. Patient recovered.

Celebrex Side Effects Report #5399488-1
Consumer or non-health professional from UNITED STATES reported CELEBREX problem on July 12, 2007. Male patient, weighting 220.0 lb, was diagnosed with inflammation, limb injury, back injury, pain and was treated with CELEBREX. After drug was administered, patient experienced the following problems/side effects: deep vein thrombosis, hypercoagulation, myocardial infarction, transient ischaemic attack, . CELEBREX dosage: unknown. During the same period patient was treated with BEXTRA, VIOXX. Patient recovered.

Cisplatin Side Effects Report #5765585-1
CISPLATIN problem was reported by a Consumer or non-health professional from UNITED STATES on June 06, 2008. Male patient, weighting 188.1 lb, was treated with CISPLATIN. After drug was administered, patient experienced the following problems/side effects: deep vein thrombosis, hypercoagulation, pulmonary embolism, tachycardia, . CISPLATIN dosage: 120 MG. During the same period patient was treated with ERBITUX, IRINOTECAN. Patient was hospitalized. Patient recovered.

Ortho Side Effects Report #5739294-9
Consumer or non-health professional from UNITED STATES reported ORTHO EVRA problem on May 09, 2008. Female patient, weighting 185.0 lb, was diagnosed with menorrhagia, contraception and was treated with ORTHO EVRA. After drug was administered, patient experienced the following problems/side effects: deep vein thrombosis, hypercoagulation, pneumonia, pulmonary embolism, venous stenosis, . ORTHO EVRA dosage: unknown. During the same period patient was treated with ORTHO EVRA. Patient was hospitalized. Patient recovered.

Warfarin Side Effects Report #5352944-4
WARFARIN problem was reported by a Consumer or non-health professional from UNITED STATES on May 07, 2007. Female patient, 83 years of age, was treated with WARFARIN. After drug was administered, patient experienced the following problems/side effects: ecchymosis, hypercoagulation, periorbital disorder, skin necrosis, . WARFARIN dosage: 4 MG, QD, PO. Patient was hospitalized. Patient recovered.

Cisplatin Side Effects Report #5293143-4
Health Professional from JAPAN reported CISPLATIN problem on Apr 09, 2007. Female patient, 29 years of age, was diagnosed with gastric cancer and was treated with CISPLATIN. After drug was administered, patient experienced the following problems/side effects: cerebrovascular accident, hypercoagulation, hypomagnesaemia, vascular injury, . CISPLATIN dosage: unknown. Patient recovered.

Randa Side Effects Report #5297424-X
RANDA problem was reported by a Health Professional from JAPAN on Apr 13, 2007. Female patient, 29 years of age, was diagnosed with gastric cancer and was treated with RANDA. After drug was administered, patient experienced the following problems/side effects: cerebrovascular accident, hypercoagulation, hypomagnesaemia, vascular injury, . RANDA dosage: unknown. Patient recovered.

Stromectol Side Effects Report #5303715-6
Physician from JAPAN reported STROMECTOL problem on Apr 11, 2007. Female patient, 70 years of age, weighting 77.16 lb, was diagnosed with acarodermatitis, prophylaxis, hypertension, arrhythmia, nausea, hyperlipidaemia, gastritis and was treated with STROMECTOL. After drug was administered, patient experienced the following problems/side effects: gastroenteritis, hypercoagulation, prescribed overdose, . STROMECTOL dosage: unknown. During the same period patient was treated with WARFARIN, AMLODIN, RYTHMODAN, LANIRAPID, GASMOTIN, MEVALOTIN, ZANTAC. Patient was hospitalized. Patient recovered.

Warfarin Side Effects Report #5638729-X
WARFARIN problem was reported by a Pharmacist from UNITED STATES on Feb 21, 2008. Male patient, 69 years of age, was diagnosed with cardiomyopathy and was treated with WARFARIN. After drug was administered, patient experienced the following problems/side effects: epistaxis, haemorrhage, hypercoagulation, injection site bruising, international normalised ratio increased, tongue discolouration, urinary tract infection, . WARFARIN dosage: 10MG DAILY PO. Patient was hospitalized. Patient recovered.

Fioricet Side Effects Report #5580732-2
Physician from GREECE reported FIORICET problem on Dec 21, 2007. Male patient, 45 years of age, was diagnosed with alcohol abuse and was treated with FIORICET. After drug was administered, patient experienced the following problems/side effects: arterial thrombosis limb, hepatic failure, hypercoagulation, overdose, peripheral ischaemia, . FIORICET dosage: unknown. During the same period patient was treated with ALCOHOL. Patient was hospitalized. Patient recovered.

Paracetamol Side Effects Report #5446486-5
PARACETAMOL problem was reported by a Physician from GREECE on Sept 04, 2007. Male patient, 45 years of age, was treated with PARACETAMOL. After drug was administered, patient experienced the following problems/side effects: hepatic failure, hypercoagulation, intentional overdose, peripheral ischaemia, . PARACETAMOL dosage: unknown. During the same period patient was treated with ALCOHOL. Patient was hospitalized. Patient recovered.

Revlimid Side Effects Report #5450935-6
Physician from UNITED STATES reported REVLIMID problem on Sept 05, 2007. Female patient, 87 years of age, was diagnosed with multiple myeloma and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: arterial thrombosis, arteriosclerosis, hypercoagulation, . REVLIMID dosage: 10 MG, 1 IN 1 D, ORAL. During the same period patient was treated with ALTAPLASE, CLOPIDOGREL, ASPIRIN. Patient was hospitalized. Patient died.

Cyclosporine Side Effects Report #5387232-3
CYCLOSPORINE problem was reported by a Consumer or non-health professional from JAPAN on July 03, 2007. Female patient, child 7 years of age, was diagnosed with nephrotic syndrome and was treated with CYCLOSPORINE. After drug was administered, patient experienced the following problems/side effects: antithrombin iii decreased, cerebral infarction, hypercoagulation, hypoalbuminaemia, muscular weakness, nephropathy toxic, nephrotic syndrome, proteinuria, speech disorder, . CYCLOSPORINE dosage: unknown. During the same period patient was treated with STEROIDS NOS. Patient was hospitalized. Patient recovered.

Cyclosporine Side Effects Report #5387232-3
Consumer or non-health professional from JAPAN reported CYCLOSPORINE problem on July 03, 2007. Female patient, child 7 years of age, was diagnosed with nephrotic syndrome and was treated with CYCLOSPORINE. After drug was administered, patient experienced the following problems/side effects: antithrombin iii decreased, cerebral infarction, hypercoagulation, hypoalbuminaemia, muscular weakness, nephropathy toxic, nephrotic syndrome, proteinuria, speech disorder, . CYCLOSPORINE dosage: unknown. During the same period patient was treated with STEROIDS NOS. Patient was hospitalized. Patient recovered.

Arava Side Effects Report #5743987-7
ARAVA problem was reported by a Physician from AUSTRALIA on May 15, 2008. Male patient was treated with ARAVA. After drug was administered, patient experienced the following problems/side effects: coagulopathy, coronary artery bypass, hypercoagulation, . ARAVA dosage: unknown. During the same period patient was treated with HEPARIN. Patient recovered.

Coumadin Side Effects Report #5752071-8
Health Professional from UNITED STATES reported COUMADIN problem on May 27, 2008. Male patient, 80 years of age, weighting 198.4 lb, was diagnosed with deep vein thrombosis, oedema, hyperglycaemia, blood cholesterol increased, prophylaxis and was treated with COUMADIN. After drug was administered, patient experienced the following problems/side effects: dehydration, gastrointestinal haemorrhage, hypercoagulation, . COUMADIN dosage: 1 FORM = 2-3 MG.. During the same period patient was treated with LASIX, GLIMEPIRIDE, LOVASTATIN, ACETYLSALICYLIC ACID SRT. Patient was hospitalized. Patient recovered.

Bleomycin Side Effects Report #5369936-1
BLEOMYCIN problem was reported by a Physician from BRAZIL on June 11, 2007. Male patient, 18 years of age, was diagnosed with testis cancer and was treated with BLEOMYCIN. After drug was administered, patient experienced the following problems/side effects: deep vein thrombosis, haemodialysis, hypercoagulation, oedema peripheral, pain in extremity, renal failure acute, renal vein thrombosis, . BLEOMYCIN dosage: unknown. During the same period patient was treated with CISPLATIN, ETOPOSIDE. Patient recovered.

Revlimid Side Effects Report #5283638-1
Pharmacist from UNITED STATES reported REVLIMID problem on Mar 29, 2007. Male patient was diagnosed with multiple myeloma and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: fall, hypercoagulation, platelet count decreased, retinal artery embolism, . REVLIMID dosage: 10MG DAILY FOR 21 DAYS PO. Patient recovered.