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FIBRIN D DIMER INCREASED side effect

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Ortho Side Effects Report #5676067-X
Consumer or non-health professional from UNITED STATES reported ORTHO EVRA problem on Mar 11, 2008. Female patient, weighting 278.0 lb, was treated with ORTHO EVRA. After drug was administered, patient experienced the following problems/side effects: fibrin d dimer increased, muscle strain, . ORTHO EVRA dosage: unknown. Patient was hospitalized. Patient recovered.

Plavix Side Effects Report #5588573-7
PLAVIX problem was reported by a Pharmacist from GERMANY on Jan 03, 2008. Male patient was treated with PLAVIX. After drug was administered, patient experienced the following problems/side effects: fibrin d dimer increased, infarction, . PLAVIX dosage: unknown. Patient was hospitalized. Patient recovered.

Champix Side Effects Report #5542815-2
Physician from FRANCE reported CHAMPIX problem on Nov 28, 2007. Female patient, weighting 123.5 lb, was diagnosed with venous stasis, orthostatic hypotension and was treated with CHAMPIX. After drug was administered, patient experienced the following problems/side effects: fibrin d dimer increased, loss of consciousness, malaise, orthostatic hypotension, pulmonary embolism, . CHAMPIX dosage: unknown. During the same period patient was treated with VELITEN. Patient was hospitalized. Patient recovered.

Desloratadine Side Effects Report #5565899-4
DESLORATADINE problem was reported by a Health Professional from SPAIN on Dec 03, 2007. Male patient, 66 years of age, was diagnosed with chronic sinusitis and was treated with DESLORATADINE. After drug was administered, patient experienced the following problems/side effects: fibrin d dimer increased, syncope, ventricular extrasystoles, . DESLORATADINE dosage: 5 MG;QD;PO. During the same period patient was treated with RINOSONE. Patient was hospitalized. Patient recovered.


Activase Side Effects Report #5569894-0
Physician from GERMANY reported ACTIVASE problem on Dec 13, 2007. Male patient was diagnosed with cerebrovascular accident and was treated with ACTIVASE. After drug was administered, patient experienced the following problems/side effects: fibrin d dimer increased, troponin increased, . ACTIVASE dosage: 60 MG/HR, UNK. Patient recovered.

Stalevo Side Effects Report #5572781-5
STALEVO problem was reported by a Consumer or non-health professional from FINLAND on Dec 11, 2007. Male patient, 76 years of age, was diagnosed with parkinson's disease, prophylaxis and was treated with STALEVO. After drug was administered, patient experienced the following problems/side effects: fibrin d dimer increased, pulmonary congestion, pulmonary embolism, pulmonary hypertension, . STALEVO dosage: unknown. During the same period patient was treated with MIRAPEXIN, ASPIRIN. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5506527-3
Physician from JAPAN reported ARIXTRA problem on Oct 30, 2007. Female patient, 64 years of age, weighting 138.9 lb, was diagnosed with thrombosis prophylaxis, insomnia and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: fibrin d dimer increased, haematocrit decreased, haemoglobin decreased, platelet count increased, post procedural haemorrhage, protein total decreased, red blood cell count decreased, vision blurred, vitreous haemorrhage, . ARIXTRA dosage: 2.5MG PER DAY. During the same period patient was treated with LOXONIN, MUCOSTA, FERROMIA, ZOLPIDEM, LENDORMIN, ADONA, HYALEIN. Patient recovered.

Champix Side Effects Report #5520781-3
CHAMPIX problem was reported by a Physician from FRANCE on Nov 07, 2007. Female patient, 34 years of age, was diagnosed with venous stasis, orthostatic hypotension and was treated with CHAMPIX. After drug was administered, patient experienced the following problems/side effects: fibrin d dimer increased, loss of consciousness, malaise, pulmonary embolism, . CHAMPIX dosage: unknown. During the same period patient was treated with VELITEN. Patient was hospitalized. Patient recovered.

Tacrolimus Side Effects Report #5477629-5
Physician from CANADA reported TACROLIMUS problem on Sept 18, 2007. Female patient, 43 years of age, was diagnosed with renal transplant and was treated with TACROLIMUS. After drug was administered, patient experienced the following problems/side effects: fibrin d dimer increased, pulmonary embolism, respiratory acidosis, . TACROLIMUS dosage: unknown. During the same period patient was treated with CORTICOSTEROIDS. Patient was hospitalized. Patient recovered.


Arixtra Side Effects Report #5483788-0
ARIXTRA problem was reported by a Physician from JAPAN on Oct 10, 2007. Female patient, 64 years of age, weighting 138.9 lb, was diagnosed with thrombosis prophylaxis, insomnia and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: fibrin d dimer increased, haematocrit decreased, haemoglobin decreased, platelet count increased, protein total decreased, red blood cell count decreased, vision blurred, vitreous haemorrhage, . ARIXTRA dosage: 2.5MG PER DAY. During the same period patient was treated with LOXONIN, MUCOSTA, FERROMIA, ZOLPIDEM, LENDORMIN, ADONA, HYALEIN. Patient recovered.

Arixtra Side Effects Report #5499395-X
Physician from JAPAN reported ARIXTRA problem on Oct 23, 2007. Female patient, 64 years of age, weighting 138.9 lb, was diagnosed with thrombosis prophylaxis, insomnia and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: fibrin d dimer increased, haematocrit decreased, haemoglobin decreased, platelet count increased, post procedural haemorrhage, protein total decreased, red blood cell count decreased, vision blurred, vitreous haemorrhage, . ARIXTRA dosage: 2.5MG PER DAY. During the same period patient was treated with LOXONIN, MUCOSTA, FERROMIA, ZOLPIDEM, LENDORMIN, ADONA, HYALEIN. Patient recovered.

Erlotinib Side Effects Report #5504062-X
ERLOTINIB problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 19, 2007. Male patient, 72 years of age, weighting 236.1 lb, was diagnosed with non-small cell lung cancer and was treated with ERLOTINIB. After drug was administered, patient experienced the following problems/side effects: fibrin d dimer increased, pulmonary embolism, . ERLOTINIB dosage: (150 MG,QD), ORAL. During the same period patient was treated with BEVACIZUMAB, VITAMIN, ATENOLOL, AMICAR. Patient recovered.

Byetta Side Effects Report #5428726-1
Consumer or non-health professional from UNITED STATES reported BYETTA problem on May 14, 2007. Male patient, 76 years of age, was diagnosed with type 2 diabetes mellitus and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: fibrin d dimer increased, joint swelling, myalgia, oedema peripheral, . BYETTA dosage: unknown. During the same period patient was treated with EXENATIDE, HUMALOG, LASIX, ACCUPRIL, ADALAT, GLUCOPHAGE, ASPIRIN, LANTUS. Patient recovered.

Byetta Side Effects Report #5428726-1
BYETTA problem was reported by a Consumer or non-health professional from UNITED STATES on May 14, 2007. Male patient, 76 years of age, was diagnosed with type 2 diabetes mellitus and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: fibrin d dimer increased, joint swelling, myalgia, oedema peripheral, . BYETTA dosage: unknown. During the same period patient was treated with EXENATIDE, HUMALOG, LASIX, ACCUPRIL, ADALAT, GLUCOPHAGE, ASPIRIN, LANTUS. Patient recovered.


Enbrel Side Effects Report #5757013-7
Physician from JAPAN reported ENBREL problem on May 26, 2008. Female patient, weighting 101.4 lb, was diagnosed with rheumatoid arthritis, essential hypertension, prophylaxis against gastrointestinal ulcer, gastric ulcer and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: fibrin d dimer increased, platelet count decreased, pneumonia, . ENBREL dosage: unknown. During the same period patient was treated with METHOTREXATE, LOXONIN, FAMOTIDINE, DICLOFENAC, NORVASC, TAKEPRON. Patient was hospitalized. Patient recovered.

Ortho Side Effects Report #5761414-0
ORTHO EVRA problem was reported by a Consumer or non-health professional from UNITED STATES on May 30, 2008. Female patient, weighting 278.0 lb, was diagnosed with menometrorrhagia and was treated with ORTHO EVRA. After drug was administered, patient experienced the following problems/side effects: fibrin d dimer increased, muscle strain, off label use, . ORTHO EVRA dosage: unknown. Patient was hospitalized. Patient recovered.

Erlotinib Side Effects Report #5732113-6
Consumer or non-health professional from JAPAN reported ERLOTINIB problem on Apr 21, 2008. Female patient, 57 years of age, was diagnosed with lung adenocarcinoma and was treated with ERLOTINIB. After drug was administered, patient experienced the following problems/side effects: fibrin d dimer increased, hepatic function abnormal, immobile, interstitial lung disease, nail disorder, no therapeutic response, pulmonary embolism, pulmonary hypertension, pulse absent, . ERLOTINIB dosage: (150 MG QD), ORAL. During the same period patient was treated with PREDNISOLONE, NIFEDIPINE, LOSARTAN POTASSIUM, FENOFIBRATE, DEPAS, RABEPRAZOLE, GASMOTIN, BASEN. Patient died on 01/23/2008.

Ortho Side Effects Report #5736302-6
ORTHO EVRA problem was reported by a Consumer or non-health professional from UNITED STATES on May 06, 2008. Female patient, weighting 278.0 lb, was diagnosed with menometrorrhagia and was treated with ORTHO EVRA. After drug was administered, patient experienced the following problems/side effects: fibrin d dimer increased, muscle strain, off label use, . ORTHO EVRA dosage: unknown. Patient was hospitalized. Patient recovered.

Ortho Side Effects Report #5744420-1
Consumer or non-health professional from UNITED STATES reported ORTHO EVRA problem on May 14, 2008. Female patient, weighting 278.0 lb, was diagnosed with menometrorrhagia and was treated with ORTHO EVRA. After drug was administered, patient experienced the following problems/side effects: fibrin d dimer increased, muscle strain, off label use, . ORTHO EVRA dosage: unknown. Patient was hospitalized. Patient recovered.


Ortho Side Effects Report #5752694-6
ORTHO EVRA problem was reported by a Consumer or non-health professional from UNITED STATES on May 27, 2008. Female patient, 27 years of age, weighting 150.0 lb, was diagnosed with contraception and was treated with ORTHO EVRA. After drug was administered, patient experienced the following problems/side effects: fibrin d dimer increased, headache, hepatic cyst, liver function test abnormal, platelet count decreased, pneumonia, pyrexia, sepsis syndrome, streptococcal infection, . ORTHO EVRA dosage: unknown. Patient was hospitalized. Patient recovered.

Thalomid Side Effects Report #5339617-9
Consumer or non-health professional from UNITED STATES reported THALOMID problem on May 25, 2007. Male patient, weighting 176.1 lb, was treated with THALOMID. After drug was administered, patient experienced the following problems/side effects: fibrin d dimer increased, pain, pleural effusion, pneumonia, pulmonary alveolar haemorrhage, pulmonary embolism, . THALOMID dosage: 5000 MG. During the same period patient was treated with ACCUTANE, TEMOZOLOMIDE. Patient was hospitalized. Patient recovered.

Varenicline Side Effects Report #5309582-9
VARENICLINE problem was reported by a Pharmacist from UNITED STATES on Apr 25, 2007. Male patient, 19 years of age, weighting 218.3 lb, was treated with VARENICLINE. After drug was administered, patient experienced the following problems/side effects: fibrin d dimer increased, pulmonary embolism, . VARENICLINE dosage: 1 MG BID PO. Patient was hospitalized. Patient recovered.

Rebif Side Effects Report #5274778-1
Health Professional from UNITED STATES reported REBIF problem on Nov 09, 2006. Female patient, 52 years of age, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: fibrin d dimer increased, hepatitis, muscle spasms, pancreatitis, . REBIF dosage: unknown. Patient died on 05/04/2006.

Oroken Side Effects Report #5657415-3
OROKEN problem was reported by a Physician from JAPAN on Mar 03, 2008. Female patient, 55 years of age, was diagnosed with vaginal infection and was treated with OROKEN. After drug was administered, patient experienced the following problems/side effects: dyspnoea, fibrin d dimer increased, nausea, . OROKEN dosage: 400MG DAILY. Patient was hospitalized. Patient recovered.

Infliximab Side Effects Report #5663973-5
Health Professional from NORWAY reported INFLIXIMAB problem on Mar 04, 2008. Female patient, weighting 231.5 lb, was diagnosed with rheumatoid arthritis and was treated with INFLIXIMAB. After drug was administered, patient experienced the following problems/side effects: dyspnoea, fibrin d dimer increased, infusion related reaction, . INFLIXIMAB dosage: 50-100 MG OF INFLIXIMAB.. During the same period patient was treated with NORSPAN, METHOTREXATE, FOLIC ACID, ACETAMINOPHEN, MOBIC, DIURETICA. Patient was hospitalized. Patient recovered.

Heparin Side Effects Report #5677099-8
HEPARIN problem was reported by a Health Professional from UNITED STATES on Mar 24, 2008. Female patient was diagnosed with flushing and was treated with HEPARIN. After drug was administered, patient experienced the following problems/side effects: activated partial thromboplastin time prolonged, fibrin d dimer increased, platelet count decreased, prothrombin time prolonged, wound secretion, . HEPARIN dosage: 100 UNITS/ML FLUSH IV. Patient was hospitalized. Patient recovered.

Memantine Side Effects Report #5619270-7
Health Professional from ITALY reported MEMANTINE problem on Jan 22, 2008. Male patient, 83 years of age, was diagnosed with dementia alzheimer's type and was treated with MEMANTINE. After drug was administered, patient experienced the following problems/side effects: bone marrow toxicity, fibrin d dimer increased, haematocrit decreased, haemoglobin decreased, leukopenia, red blood cell count decreased, thrombocytopenia, . MEMANTINE dosage: 20 MG QD PO. During the same period patient was treated with METFORMIN, RAMIPRIL, TRAZODONE. Patient recovered.

Tysabri Side Effects Report #5623335-3
TYSABRI problem was reported by a Physician from UNITED STATES on Feb 01, 2008. Female patient, 58 years of age, weighting 171.0 lb, was diagnosed with multiple sclerosis and was treated with TYSABRI. After drug was administered, patient experienced the following problems/side effects: chest pain, fibrin d dimer increased, pulmonary embolism, . TYSABRI dosage: 300 MG;QM;IV. Patient was hospitalized. Patient recovered.

Rituxan Side Effects Report #5603004-6
Physician from JAPAN reported RITUXAN problem on Jan 17, 2008. Female patient, weighting 149.9 lb, was diagnosed with systemic lupus erythematosus and was treated with RITUXAN. After drug was administered, patient experienced the following problems/side effects: diarrhoea, fibrin d dimer increased, platelet count decreased, pyrexia, urticaria, vomiting, . RITUXAN dosage: 500 MG, QD. During the same period patient was treated with ULCERLMIN, PRECIPITATED CALCIUM CARBONATE, ROCALTROL, ACTONEL, OMEPRAL, CYTOTEC, MAGNESIUM OXIDE. Patient was hospitalized. Patient recovered.

Lapatinib Side Effects Report #5475825-4
LAPATINIB problem was reported by a Physician from UNITED KINGDOM on Sept 27, 2007. Female patient, 54 years of age, weighting 154.3 lb, was diagnosed with breast cancer metastatic and was treated with LAPATINIB. After drug was administered, patient experienced the following problems/side effects: deep vein thrombosis, fibrin d dimer increased, pleuritic pain, . LAPATINIB dosage: 750MG PER DAY. During the same period patient was treated with CAPECITABINE. Patient was hospitalized. Patient recovered.

Nuvaring Side Effects Report #5489519-2
Pharmacist from UNITED STATES reported NUVARING problem on Oct 16, 2007. Female patient, 22 years of age, weighting 126.8 lb, was diagnosed with contraception and was treated with NUVARING. After drug was administered, patient experienced the following problems/side effects: dyspnoea, fibrin d dimer increased, pulmonary embolism, . NUVARING dosage: unknown. Patient was hospitalized. Patient recovered.

Lapatinib Side Effects Report #5453869-6
LAPATINIB problem was reported by a Physician from UNITED KINGDOM on Sept 10, 2007. Female patient, 54 years of age, weighting 154.3 lb, was treated with LAPATINIB. After drug was administered, patient experienced the following problems/side effects: deep vein thrombosis, fibrin d dimer increased, pleuritic pain, . LAPATINIB dosage: 750MG PER DAY. During the same period patient was treated with CAPECITABINE. Patient was hospitalized. Patient recovered.

Sulfamethoxazole Side Effects Report #5455509-9
Consumer or non-health professional from UNITED STATES reported SULFAMETHOXAZOLE AND TRIMETHOPRIM problem on Aug 22, 2007. Male patient, 43 years of age, weighting 160.0 lb, was diagnosed with subcutaneous abscess and was treated with SULFAMETHOXAZOLE AND TRIMETHOPRIM. After drug was administered, patient experienced the following problems/side effects: dry mouth, fibrin d dimer increased, flank pain, furuncle, hypercoagulation, movement disorder, muscle spasms, nausea, pleuritic pain, . SULFAMETHOXAZOLE AND TRIMETHOPRIM dosage: unknown. During the same period patient was treated with METHADONE. Patient was hospitalized. Patient recovered.

Copaxone Side Effects Report #5387147-0
COPAXONE problem was reported by a Health Professional from UNITED STATES on July 02, 2007. Female patient, 30 years of age, weighting 233.0 lb, was diagnosed with multiple sclerosis and was treated with COPAXONE. After drug was administered, patient experienced the following problems/side effects: embolism, fibrin d dimer increased, haematocrit decreased, haemoglobin decreased, thromboangiitis obliterans, vasculitis, white blood cell count increased, . COPAXONE dosage: (20 MG), SUBCUTANEOUS. During the same period patient was treated with NIFEDIPINE, DYAZIDE, LISINOPRIL, LABETALOL, NAPROXEN, VICODIN. Patient recovered.

Copaxone Side Effects Report #5387147-0
Health Professional from UNITED STATES reported COPAXONE problem on July 02, 2007. Female patient, 30 years of age, weighting 233.0 lb, was diagnosed with multiple sclerosis and was treated with COPAXONE. After drug was administered, patient experienced the following problems/side effects: embolism, fibrin d dimer increased, haematocrit decreased, haemoglobin decreased, thromboangiitis obliterans, vasculitis, white blood cell count increased, . COPAXONE dosage: (20 MG), SUBCUTANEOUS. During the same period patient was treated with NIFEDIPINE, DYAZIDE, LISINOPRIL, LABETALOL, NAPROXEN, VICODIN. Patient recovered.

Novoseven Side Effects Report #5753427-X
NOVOSEVEN problem was reported by a Physician from JAPAN on May 19, 2008. Male patient, 67 years of age, weighting 125.7 lb, was diagnosed with acquired haemophilia, diabetes mellitus, hypothyroidism, osteoporosis prophylaxis, renal failure, prophylaxis against gastrointestinal ulcer and was treated with NOVOSEVEN. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, fibrin d dimer increased, hepatic function abnormal, hypoproteinaemia, platelet count decreased, renal failure, subcutaneous haematoma, white blood cell count increased, . NOVOSEVEN dosage: 2.4 - 9.6 MG. During the same period patient was treated with NOVOLIN R, PREDONINE, THYRADIN S, ONEALFA, DIOVAN, LASIX, TAKEPRON. Patient died on 04/29/2008.

Mirena Side Effects Report #5714082-8
Physician from GERMANY reported MIRENA problem on Apr 10, 2008. Female patient, 38 years of age, weighting 136.7 lb, was diagnosed with contraception and was treated with MIRENA. After drug was administered, patient experienced the following problems/side effects: acne, fibrin d dimer increased, headache, hemianopia, malaise, night sweats, weight increased, . MIRENA dosage: unknown. Patient was hospitalized. Patient recovered.

Mirena Side Effects Report #5720615-8
MIRENA problem was reported by a Physician from GERMANY on Apr 10, 2008. Female patient, 38 years of age, weighting 136.7 lb, was diagnosed with contraception and was treated with MIRENA. After drug was administered, patient experienced the following problems/side effects: acne, fibrin d dimer increased, headache, hemianopia, malaise, night sweats, weight increased, . MIRENA dosage: unknown. Patient was hospitalized. Patient recovered.

Gonal Side Effects Report #5315176-1
Consumer or non-health professional from FRANCE reported GONAL problem on Apr 16, 2007. Female patient, 37 years of age, weighting 154.3 lb, was diagnosed with in vitro fertilisation and was treated with GONAL. After drug was administered, patient experienced the following problems/side effects: anti factor x antibody positive, fibrin d dimer increased, hypocapnia, pleural effusion, pulmonary embolism, . GONAL dosage: unknown. Patient was hospitalized. Patient recovered.

Cymbalta Side Effects Report #5338505-1
CYMBALTA problem was reported by a Health Professional from UNITED STATES on Nov 06, 2006. Female patient, 33 years of age, was treated with CYMBALTA. After drug was administered, patient experienced the following problems/side effects: confusional state, fibrin d dimer increased, . CYMBALTA dosage: 60 MG. Patient recovered.

Gleevec Side Effects Report #5669304-9
Physician from JAPAN reported GLEEVEC problem on Mar 05, 2008. Female patient, 66 years of age, weighting 130.1 lb, was diagnosed with acute lymphocytic leukaemia, osteoporosis prophylaxis and was treated with GLEEVEC. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, disseminated intravascular coagulation, fibrin d dimer increased, fibrin decreased, fibrin degradation products increased, gastric haemorrhage, haemoglobin decreased, haemolytic anaemia, melaena, . GLEEVEC dosage: 600 MG/DAY. During the same period patient was treated with PREDNISOLONE, BONALON. Patient recovered.

Winrho Side Effects Report #5677840-4
WINRHO SDF problem was reported by a Physician from UNITED STATES on Mar 03, 2008. Female patient, 59 years of age, weighting 220.5 lb, was diagnosed with idiopathic thrombocytopenic purpura and was treated with WINRHO SDF. After drug was administered, patient experienced the following problems/side effects: asthenia, back pain, fibrin d dimer increased, haemodialysis, haemoglobin urine present, haemolytic anaemia, intravascular haemolysis, renal failure, . WINRHO SDF dosage: unknown. During the same period patient was treated with METHADONE. Patient was hospitalized. Patient recovered.

Prezolon Side Effects Report #5624216-1
Consumer or non-health professional from GREECE reported PREZOLON problem on Feb 08, 2008. Female patient, child 7 years of age, was diagnosed with vasculitis and was treated with PREZOLON. After drug was administered, patient experienced the following problems/side effects: activated partial thromboplastin time prolonged, blood urea increased, fibrin d dimer increased, haematocrit decreased, haemoglobin decreased, histiocytosis haematophagic, immunosuppression, parvovirus b19 serology positive, parvovirus infection, . PREZOLON dosage: unknown. During the same period patient was treated with METHYLPREDNISOLONE, KINERET, CORTICOSTEROIDS, METHOTREXATE, CYCLOPHOSPHAMIDE, ENBREL, AZATHIOPRINE, SANDIMMUNE. Patient died on 05/12/2007.

Gleevec Side Effects Report #5591080-9
GLEEVEC problem was reported by a Physician from JAPAN on Jan 08, 2008. Female patient, 66 years of age, weighting 130.1 lb, was diagnosed with acute lymphocytic leukaemia, osteoporosis prophylaxis and was treated with GLEEVEC. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, disseminated intravascular coagulation, fibrin d dimer increased, fibrin decreased, fibrin degradation products increased, gastric haemorrhage, haemoglobin decreased, haemolytic anaemia, melaena, . GLEEVEC dosage: 600 MG/DAY. During the same period patient was treated with PREDNISOLONE, BONALON. Patient recovered.

Norinyl Side Effects Report #5599733-3
Pharmacist from UNITED STATES reported NORINYL problem on Jan 18, 2008. Female patient, 37 years of age, weighting 209.4 lb, was diagnosed with oral contraception and was treated with NORINYL. After drug was administered, patient experienced the following problems/side effects: chest pain, fibrin d dimer increased, international normalised ratio decreased, pregnancy, pulmonary embolism, . NORINYL dosage: unknown. During the same period patient was treated with ALLEGRA, FLONASE, NAPROXEN, PERCOCET. Patient was hospitalized. Patient recovered.

Fluoxetine Side Effects Report #5602182-2
FLUOXETINE problem was reported by a Consumer or non-health professional from ITALY on Jan 10, 2008. Female patient, 28 years of age, was diagnosed with eating disorder, migraine and was treated with FLUOXETINE. After drug was administered, patient experienced the following problems/side effects: confusional state, fibrin d dimer increased, grand mal convulsion, loss of consciousness, mental disorder, renal failure acute, rhabdomyolysis, serotonin syndrome, . FLUOXETINE dosage: 60 MG; QD, 20 MG; QD. During the same period patient was treated with ELETRIPTAN HYDROBROMIDE, HYPERICUM PERFORATUM, AMITRIPTYLINE. Patient was hospitalized. Patient recovered.

Geodon Side Effects Report #5512120-9
Consumer or non-health professional from UNITED STATES reported GEODON problem on Nov 05, 2007. Male patient, weighting 126.1 lb, was diagnosed with mood altered and was treated with GEODON. After drug was administered, patient experienced the following problems/side effects: depression, dysarthria, fibrin d dimer increased, pulmonary embolism, transient ischaemic attack, . GEODON dosage: TEXT:20MG. During the same period patient was treated with ARICEPT, PRAVASTATIN, FEXOFENADINE, DIGITEK. Patient was hospitalized. Patient recovered.

Follitropin Side Effects Report #5513555-0
FOLLITROPIN ALPHA problem was reported by a Consumer or non-health professional from JAPAN on Oct 24, 2007. Female patient, 34 years of age, was diagnosed with ovulation induction and was treated with FOLLITROPIN ALPHA. After drug was administered, patient experienced the following problems/side effects: ascites, fibrin d dimer increased, fibrin degradation products increased, hepatic enzyme increased, inflammation, jugular vein thrombosis, multiple pregnancy, ovarian hyperstimulation syndrome, . FOLLITROPIN ALPHA dosage: unknown. During the same period patient was treated with MENOTROPINS, CHORIONIC GONADTROPIN. Patient was hospitalized. Patient recovered.

Phenylephrine Side Effects Report #5525725-6
Consumer or non-health professional from UNITED STATES reported PHENYLEPHRINE HYDROCHLORIDEECTION problem on Nov 07, 2007. Male patient, 45 years of age, was treated with PHENYLEPHRINE HYDROCHLORIDEECTION. After drug was administered, patient experienced the following problems/side effects: biopsy skin abnormal, blood blister, fibrin d dimer increased, hypoaesthesia, platelet count decreased, purpura, rash, skin discolouration, skin exfoliation, . PHENYLEPHRINE HYDROCHLORIDEECTION dosage: unknown. During the same period patient was treated with LEVOFLOXACIN, QUINUPRISTIN, HYDROCORTISONE SUCCINATE, PROPOFOL, MIDAZOLAM, ELECTROLYTE, FUROSEMIDE, HYDROXYZINE. Patient recovered.

Crestor Side Effects Report #5478247-5
CRESTOR problem was reported by a Health Professional from UNITED STATES on Sept 25, 2007. Female patient, 61 years of age, was treated with CRESTOR. After drug was administered, patient experienced the following problems/side effects: chest pain, dyspnoea, fibrin d dimer increased, hepatic enzyme increased, hypoxia, myalgia, reflux oesophagitis, . CRESTOR dosage: unknown. During the same period patient was treated with ASPIRIN, ACIPHEX, ANTIVERT, DETROL LA, IMITREX, LODINE, LYRICA. Patient was hospitalized. Patient recovered.

Prezolon Side Effects Report #5485173-4
Consumer or non-health professional from GREECE reported PREZOLON problem on Oct 09, 2007. Female patient, child 7 years of age, was diagnosed with vasculitis and was treated with PREZOLON. After drug was administered, patient experienced the following problems/side effects: activated partial thromboplastin time prolonged, blood urea increased, fibrin d dimer increased, haematocrit decreased, haemoglobin decreased, histiocytosis haematophagic, immunosuppression, parvovirus b19 serology positive, parvovirus infection, . PREZOLON dosage: unknown. During the same period patient was treated with METHYLPREDNISOLONE, KINERET, CORTICOSTEROIDS, METHOTREXATE, CYCLOPHOSPHAMIDE, ENBREL, AZATHIOPRINE, SANDIMMUNE. Patient died on 05/12/2007.