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ANTIPHOSPHOLIPID SYNDROME side effect

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Myfortic Side Effects Report #5653083-5
Consumer or non-health professional from SPAIN reported MYFORTIC problem on Feb 26, 2008. Male patient, 51 years of age, weighting 171.1 lb, was diagnosed with renal transplant and was treated with MYFORTIC. After drug was administered, patient experienced the following problems/side effects: antiphospholipid syndrome, bacteraemia, bone marrow disorder, complications of transplanted kidney, haemolytic anaemia, leukopenia, myelodysplastic syndrome, obstructive airways disorder, pancytopenia, . MYFORTIC dosage: 720 MG/DAILY. During the same period patient was treated with VALCYTE, PREDNISONE, PROGRAF. Patient was hospitalized. Patient recovered.

Fosamax Side Effects Report #5664626-X
FOSAMAX problem was reported by a Physician from UNITED STATES on Mar 05, 2008. Female patient, 40 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: antiphospholipid syndrome, anxiety, cerebrovascular accident, connective tissue disorder, convulsion, cranial nerve disorder, deep vein thrombosis, fall, leukopenia, . FOSAMAX dosage: unknown. Patient was hospitalized. Patient recovered.

Fosamax Side Effects Report #5670851-4
Physician from UNITED STATES reported FOSAMAX problem on Mar 07, 2008. Female patient, 40 years of age, weighting 134.5 lb, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: antiphospholipid syndrome, anxiety, cerebrovascular accident, connective tissue disorder, constipation, convulsion, cranial nerve disorder, deep vein thrombosis, . FOSAMAX dosage: unknown. Patient was hospitalized. Patient recovered.

Myfortic Side Effects Report #5674167-1
MYFORTIC problem was reported by a Consumer or non-health professional from SPAIN on Mar 12, 2008. Male patient, 51 years of age, weighting 171.1 lb, was diagnosed with renal transplant and was treated with MYFORTIC. After drug was administered, patient experienced the following problems/side effects: antiphospholipid syndrome, bacteraemia, bone marrow disorder, complications of transplanted kidney, haemolytic anaemia, leukopenia, myelodysplastic syndrome, obstructive airways disorder, pancytopenia, . MYFORTIC dosage: 720 MG/DAILY. During the same period patient was treated with VALCYTE, PREDNISONE, PROGRAF. Patient was hospitalized. Patient recovered.


Cyclophosphamide Side Effects Report #5676269-2
Consumer or non-health professional from reported CYCLOPHOSPHAMIDE problem on Mar 17, 2008. Female patient, 16 years of age, was diagnosed with focal glomerulosclerosis, systemic lupus erythematosus, antiphospholipid syndrome, lupus nephritis and was treated with CYCLOPHOSPHAMIDE. After drug was administered, patient experienced the following problems/side effects: antiphospholipid syndrome, arterial thrombosis, focal glomerulosclerosis, myocarditis, proteinuria, stevens-johnson syndrome, . CYCLOPHOSPHAMIDE dosage: unknown. During the same period patient was treated with PREDNISONE, AZATHIOPRINE USP, MYCOPHENOLATE MOFETIL, MYCOPHENOLATE MOFETIL, RITUXIMAB, HEPARIN. Patient recovered.

Magnevist Side Effects Report #5590990-6
MAGNEVIST problem was reported by a Physician from UNITED STATES on Jan 03, 2008. Female patient, 44 years of age, weighting 198.4 lb, was diagnosed with nuclear magnetic resonance imaging and was treated with MAGNEVIST. After drug was administered, patient experienced the following problems/side effects: antiphospholipid syndrome, cardiac failure congestive, catheter related infection, catheter sepsis, graft thrombosis, hypotension, large intestine perforation, metabolic alkalosis, . MAGNEVIST dosage: unknown. During the same period patient was treated with COUMADIN. Patient died on 04/28/2007.

Fosamax Side Effects Report #5595313-4
Physician from UNITED STATES reported FOSAMAX problem on Jan 10, 2008. Female patient, 36 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: antiphospholipid syndrome, benign neoplasm, bronchitis, complex partial seizures, dehydration, dysaesthesia, encephalitis, gastroenteritis, hepatitis, . FOSAMAX dosage: unknown. During the same period patient was treated with PREDNISONE, NEURONTIN, PLAVIX, ASPIRIN, ADVAIR DISKUS, ALBUTEROL, MS CONTIN, TOPAMAX. Patient was hospitalized. Patient recovered.

Myfortic Side Effects Report #5608050-4
MYFORTIC problem was reported by a Physician from SPAIN on Jan 21, 2008. Male patient, 51 years of age, weighting 171.1 lb, was diagnosed with renal transplant and was treated with MYFORTIC. After drug was administered, patient experienced the following problems/side effects: antiphospholipid syndrome, bacteraemia, bone marrow disorder, haemolytic anaemia, leukopenia, myelodysplastic syndrome, obstructive airways disorder, pancytopenia, parotitis, . MYFORTIC dosage: 720 MG/DAILY. During the same period patient was treated with VALCYTE, PREDNISONE, PROGRAF. Patient was hospitalized. Patient recovered.

Fosamax Side Effects Report #5556118-3
Physician from UNITED STATES reported FOSAMAX problem on Dec 05, 2007. Female patient, 40 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: antiphospholipid syndrome, anxiety, cerebrovascular accident, connective tissue disorder, cranial nerve disorder, deep vein thrombosis, fall, leukopenia, meningitis viral, . FOSAMAX dosage: unknown. Patient was hospitalized. Patient recovered.


Fosamax Side Effects Report #5567474-4
FOSAMAX problem was reported by a Physician from UNITED STATES on Dec 13, 2007. Female patient, 40 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: antiphospholipid syndrome, anxiety, cerebrovascular accident, connective tissue disorder, cranial nerve disorder, deep vein thrombosis, fall, leukopenia, meningitis viral, . FOSAMAX dosage: unknown. Patient was hospitalized. Patient recovered.

Myfortic Side Effects Report #5577665-4
Physician from SPAIN reported MYFORTIC problem on Dec 21, 2007. Male patient, 51 years of age, weighting 171.1 lb, was diagnosed with renal transplant and was treated with MYFORTIC. After drug was administered, patient experienced the following problems/side effects: antiphospholipid syndrome, bone marrow disorder, haemolytic anaemia, leukopenia, myelodysplastic syndrome, pancytopenia, pyrexia, spleen operation, therapeutic embolisation, . MYFORTIC dosage: 720 MG/DAILY. During the same period patient was treated with VALCYTE, PREDNISONE. Patient was hospitalized. Patient recovered.

Fosamax Side Effects Report #5508955-9
FOSAMAX problem was reported by a Physician from UNITED STATES on Oct 31, 2007. Female patient, 40 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: antiphospholipid syndrome, anxiety, autoimmune disorder, cerebrovascular accident, connective tissue disorder, deep vein thrombosis, fall, leukopenia, meningitis viral, . FOSAMAX dosage: unknown. Patient was hospitalized. Patient recovered.

Sertraline Side Effects Report #5511748-X
Physician from UNITED KINGDOM reported SERTRALINE problem on Oct 29, 2007. Female patient, weighting 138.9 lb, was diagnosed with depression, asthma, constipation, crohn's disease and was treated with SERTRALINE. After drug was administered, patient experienced the following problems/side effects: antiphospholipid syndrome, stillbirth, vaginal haemorrhage, . SERTRALINE dosage: DAILY DOSE:50MG. During the same period patient was treated with VITAMINS, ALBUTEROL, LACTULOSE, BECLOMETHASONE DIPROPIONATE, KETOVITE, INFLUENZA VACCINE, CERAZETTE. Patient recovered.

Fosamax Side Effects Report #5521026-0
FOSAMAX problem was reported by a Physician from UNITED STATES on Nov 13, 2007. Female patient, 40 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: antiphospholipid syndrome, anxiety, cerebrovascular accident, connective tissue disorder, cranial nerve disorder, deep vein thrombosis, fall, leukopenia, meningitis viral, . FOSAMAX dosage: unknown. Patient was hospitalized. Patient recovered.


Methylprednisolo Side Effects Report #5531266-2
Consumer or non-health professional from SLOVAKIA (Slovak Republic) reported METHYLPREDNISOLONE problem on Nov 13, 2007. Male patient, 48 years of age, was diagnosed with hypertension and was treated with METHYLPREDNISOLONE. After drug was administered, patient experienced the following problems/side effects: antiphospholipid syndrome, cerebral haemorrhage, condition aggravated, extremity necrosis, pain, renal tubular necrosis, . METHYLPREDNISOLONE dosage: 500 MG, QD; INTRAVENOUS. During the same period patient was treated with HEPARIN, ANTIBACTERIALS SYSTEMIC USE, EPOPROSTENOL, URAPIDIL, FRESH FROZEN PLASMA. Patient was hospitalized. Patient died.

Arixtra Side Effects Report #5466654-6
ARIXTRA problem was reported by a Pharmacist from UNITED STATES on Sept 21, 2007. Female patient, 46 years of age, was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: antiphospholipid syndrome, thrombocytopenia, . ARIXTRA dosage: unknown. Patient recovered.

Fosamax Side Effects Report #5470950-6
Physician from UNITED STATES reported FOSAMAX problem on Sept 21, 2007. Female patient, 40 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: antiphospholipid syndrome, anxiety, cerebrovascular accident, connective tissue disorder, deep vein thrombosis, fall, leukopenia, meningitis viral, musculoskeletal pain, . FOSAMAX dosage: unknown. Patient was hospitalized. Patient recovered.

Avonex Side Effects Report #5384895-3
AVONEX problem was reported by a Consumer or non-health professional from UNITED STATES on June 22, 2007. Female patient, 38 years of age, weighting 206.0 lb, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: antiphospholipid syndrome, autoimmune hepatitis, fitz-hugh-curtis syndrome, hepatic steatosis, migraine, multiple sclerosis, transient ischaemic attack, . AVONEX dosage: unknown. Patient recovered.

Avonex Side Effects Report #5384895-3
Consumer or non-health professional from UNITED STATES reported AVONEX problem on June 22, 2007. Female patient, 38 years of age, weighting 206.0 lb, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: antiphospholipid syndrome, autoimmune hepatitis, fitz-hugh-curtis syndrome, hepatic steatosis, migraine, multiple sclerosis, transient ischaemic attack, . AVONEX dosage: unknown. Patient recovered.


Remicade Side Effects Report #5762181-7
REMICADE problem was reported by a Physician from UNITED STATES on May 30, 2008. Male patient was diagnosed with colitis ulcerative, inferior vena caval occlusion, antiphospholipid syndrome and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: antiphospholipid syndrome, aqueductal stenosis, graft versus host disease, hepatosplenic t-cell lymphoma, hydrocephalus, hypertension, nuclear magnetic resonance imaging brain abnormal, pulmonary embolism, . REMICADE dosage: unknown. During the same period patient was treated with IMURAN, LOVENOX, ASACOL, LOW MOLECULAR WEIGHT HEPARIN, LOW MOLECULAR WEIGHT HEPARIN, STEROIDS. Patient died.

Menotrophin Side Effects Report #5798827-7
Physician from SERBIA reported MENOTROPHIN problem on Feb 25, 2008. Female patient, 28 years of age, was diagnosed with anovulatory cycle and was treated with MENOTROPHIN. After drug was administered, patient experienced the following problems/side effects: antiphospholipid syndrome, beta-2 glycoprotein antibody positive, blood immunoglobulin g increased, blood immunoglobulin m increased, cardiac myxoma, complement factor c3 increased, complement factor c4 increased, complication of pregnancy, hirsutism, . MENOTROPHIN dosage: unknown. During the same period patient was treated with CHORIOANIC GONADOTROPIN, CLOMIPHENE ACETATE, ESTROGEN. Patient was hospitalized. Patient recovered.

Fosamax Side Effects Report #5728974-7
FOSAMAX problem was reported by a Physician from UNITED STATES on Apr 30, 2008. Female patient, 39 years of age, weighting 198.4 lb, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: antiphospholipid syndrome, anxiety, arthralgia, arthropathy, cerebrovascular accident, connective tissue disorder, constipation, convulsion, . FOSAMAX dosage: unknown. Patient was hospitalized. Patient recovered.

Myfortic Side Effects Report #5690145-0
Consumer or non-health professional from SPAIN reported MYFORTIC problem on Mar 26, 2008. Male patient, 51 years of age, weighting 171.1 lb, was diagnosed with renal transplant and was treated with MYFORTIC. After drug was administered, patient experienced the following problems/side effects: antiphospholipid syndrome, bacteraemia, bone marrow disorder, complications of transplanted kidney, haemolytic anaemia, leukopenia, myelodysplastic syndrome, obstructive airways disorder, pancytopenia, . MYFORTIC dosage: 720 MG/DAILY. During the same period patient was treated with VALCYTE, PREDNISONE, PROGRAF. Patient was hospitalized. Patient recovered.

Abatacept Side Effects Report #5693777-9
ABATACEPT problem was reported by a Health Professional from UNITED STATES on Mar 21, 2008. Female patient, 54 years of age, was diagnosed with crohn's disease, gastrooesophageal reflux disease, anaemia, insomnia, rectal spasm, inflammatory bowel disease, abdominal pain, menopausal symptoms, vitamin supplementation and was treated with ABATACEPT. After drug was administered, patient experienced the following problems/side effects: antiphospholipid syndrome, deep vein thrombosis, . ABATACEPT dosage: unknown. During the same period patient was treated with PREVACID, FERREX, TEMAZEPAM, CANASA, PREDNISONE, NULEV, VAGIFEM, CENTRUM. Patient was hospitalized. Patient recovered.

Remicade Side Effects Report #5329921-2
Health Professional from UNITED STATES reported REMICADE problem on May 08, 2007. Male patient was diagnosed with colitis ulcerative, inferior vena caval occlusion, antiphospholipid syndrome and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: antiphospholipid syndrome, cerebral ventricle dilatation, graft versus host disease, hepatosplenic t-cell lymphoma, hydrocephalus, hypertension, nuclear magnetic resonance imaging brain abnormal, pulmonary embolism, . REMICADE dosage: unknown. During the same period patient was treated with IMURAN, LOVENOX, ASACOL, LOW MOLECULAR WEIGHT HEPARIN, LOW MOLECULAR WEIGHT HEPARIN, STEROIDS. Patient recovered.

Rebif Side Effects Report #5330186-6
REBIF problem was reported by a Consumer or non-health professional from UNITED STATES on May 04, 2007. Female patient, 48 years of age, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: antiphospholipid syndrome, . REBIF dosage: unknown. Patient recovered.

Rebif Side Effects Report #5339959-7
Consumer or non-health professional from UNITED STATES reported REBIF problem on May 16, 2007. Female patient, 48 years of age, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: antiphospholipid syndrome, . REBIF dosage: unknown. Patient recovered.

Alteplase Side Effects Report #5266728-9
ALTEPLASE problem was reported by a Physician from GERMANY on Mar 01, 2007. Female patient, 26 years of age, was diagnosed with cerebral artery occlusion and was treated with ALTEPLASE. After drug was administered, patient experienced the following problems/side effects: antiphospholipid syndrome, cerebral artery occlusion, ischaemic cerebral infarction, premature labour, . ALTEPLASE dosage: 0.9 MG/KG, SINGLE, INTRAVENOUS. Patient was hospitalized. Patient recovered.

Raptiva Side Effects Report #5278514-4
Physician from UNITED STATES reported RAPTIVA problem on Mar 14, 2007. Male patient, 47 years of age, was diagnosed with psoriasis and was treated with RAPTIVA. After drug was administered, patient experienced the following problems/side effects: antiphospholipid syndrome, deep vein thrombosis, . RAPTIVA dosage: 1 ML, 1/WEEK, SUBCUTANEOUS. During the same period patient was treated with WATER. Patient recovered.

Chlorpromazine Side Effects Report #5281127-1
CHLORPROMAZINE problem was reported by a Physician from UNITED KINGDOM on Mar 13, 2007. Female patient, 38 years of age, was diagnosed with schizoaffective disorder and was treated with CHLORPROMAZINE. After drug was administered, patient experienced the following problems/side effects: antiphospholipid syndrome, confusional state, encephalopathy, grand mal convulsion, hypoventilation, paralysis, somnolence, status epilepticus, thrombocytopenia, . CHLORPROMAZINE dosage: unknown. Patient was hospitalized. Patient recovered.

Humira Side Effects Report #5677670-3
Consumer or non-health professional from FRANCE reported HUMIRA problem on Mar 14, 2008. Male patient, weighting 202.8 lb, was diagnosed with rheumatoid arthritis, osteoporosis prophylaxis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: agranulocytosis, antiphospholipid syndrome, neutropenia, thrombocytopenia, . HUMIRA dosage: unknown. During the same period patient was treated with COMMERCIAL HUMIRA, PARACETAMOL, PREDNISONE, RISEDRONATE, LEKOVIT CA. Patient recovered.

Avonex Side Effects Report #5567858-4
AVONEX problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 05, 2007. Female patient, 38 years of age, weighting 206.0 lb, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: antinuclear antibody positive, antiphospholipid syndrome, aphonia, autoimmune hepatitis, cerebrovascular accident, condition aggravated, fitz-hugh-curtis syndrome, hepatic steatosis, hypoaesthesia facial, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.

Infliximab Side Effects Report #5570700-9
Health Professional from FRANCE reported INFLIXIMAB problem on Dec 06, 2007. Female patient, 67 years of age, was diagnosed with pustular psoriasis and was treated with INFLIXIMAB. After drug was administered, patient experienced the following problems/side effects: antinuclear antibody positive, antiphospholipid syndrome, dna antibody positive, pustular psoriasis, . INFLIXIMAB dosage: unknown. During the same period patient was treated with METHOTREXATE, ETANERCEPT. Patient recovered.

Follitropin Side Effects Report #5407999-5
FOLLITROPIN ALPHA problem was reported by a Consumer or non-health professional from SPAIN on July 25, 2007. Female patient, 35 years of age, was diagnosed with assisted fertilisation and was treated with FOLLITROPIN ALPHA. After drug was administered, patient experienced the following problems/side effects: acute myocardial infarction, antiphospholipid syndrome, aortic aneurysm, aortic valve calcification, aortic valve disease, aortic valve incompetence, aortic valve stenosis, aphasia, cerebral ischaemia, . FOLLITROPIN ALPHA dosage: unknown. During the same period patient was treated with MENOTROPHIN. Patient was hospitalized. Patient recovered.

Wytens Side Effects Report #5414920-2
Consumer or non-health professional from FRANCE reported WYTENS problem on July 26, 2007. Female patient, 71 years of age, was diagnosed with hypertension and was treated with WYTENS. After drug was administered, patient experienced the following problems/side effects: anaemia haemolytic autoimmune, antiphospholipid syndrome, coombs positive haemolytic anaemia, cytolytic hepatitis, double stranded dna antibody, hyperproteinaemia, systemic lupus erythematosus, . WYTENS dosage: unknown. During the same period patient was treated with RABEPRAZOLE, XANAX. Patient was hospitalized. Patient recovered.

Hrdrochlorothiaz Side Effects Report #5386419-3
HRDROCHLOROTHIAZIDE problem was reported by a Consumer or non-health professional from UNITED STATES on July 10, 2007. Female patient, 53 years of age, weighting 220.0 lb, was diagnosed with blood pressure and was treated with HRDROCHLOROTHIAZIDE. After drug was administered, patient experienced the following problems/side effects: acute respiratory distress syndrome, antiphospholipid syndrome, condition aggravated, gait disturbance, joint swelling, lung disorder, myocardial infarction, oedema peripheral, renal disorder, . HRDROCHLOROTHIAZIDE dosage: unknown. Patient was hospitalized. Patient recovered.

Hrdrochlorothiaz Side Effects Report #5386419-3
Consumer or non-health professional from UNITED STATES reported HRDROCHLOROTHIAZIDE problem on July 10, 2007. Female patient, 53 years of age, weighting 220.0 lb, was diagnosed with blood pressure and was treated with HRDROCHLOROTHIAZIDE. After drug was administered, patient experienced the following problems/side effects: acute respiratory distress syndrome, antiphospholipid syndrome, condition aggravated, gait disturbance, joint swelling, lung disorder, myocardial infarction, oedema peripheral, renal disorder, . HRDROCHLOROTHIAZIDE dosage: unknown. Patient was hospitalized. Patient recovered.

Humira Side Effects Report #5765797-7
HUMIRA problem was reported by a Pharmacist from UNITED STATES on June 02, 2008. Female patient, weighting 147.0 lb, was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: agranulocytosis, antiphospholipid syndrome, arterial stenosis, arterial stenosis limb, arteriosclerosis, bone marrow failure, burning sensation, erythropoiesis abnormal, foetal haemoglobin increased, . HUMIRA dosage: unknown. During the same period patient was treated with LEFLUNOMIDE, METOPROLOL SUCCINATE, LOSARTAN POTASSIUM, CLOPIDOGREL, ASPIRIN, ESOMEPRAZOLE MAGNESIUM, GLYBURIDE. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5767396-X
Physician from GERMANY reported ARIXTRA problem on June 09, 2008. Female patient, 53 years of age, was diagnosed with thrombosis prophylaxis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: angina pectoris, antiphospholipid syndrome, arthralgia, cardiac disorder, deep vein thrombosis, diabetes mellitus inadequate control, diarrhoea, fibromyalgia, hypertension, . ARIXTRA dosage: 2.5MG PER DAY. During the same period patient was treated with CLEXANE, GABAPENTIN, SYNTESTAN, NEXIUM, DELIX, KETOF, VENTILASTIN NOVOLIZER. Patient recovered.

Arixtra Side Effects Report #5745253-2
ARIXTRA problem was reported by a Physician from GERMANY on May 14, 2008. Female patient, 53 years of age, was diagnosed with thrombosis prophylaxis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: angina pectoris, antiphospholipid syndrome, arthralgia, cardiac disorder, deep vein thrombosis, diabetes mellitus inadequate control, diarrhoea, fibromyalgia, hypertension, . ARIXTRA dosage: 2.5MG PER DAY. During the same period patient was treated with CLEXANE, GABAPENTIN, SYNTESTAN, NEXIUM, DELIX, KETOF, VENTILASTIN NOVOLIZER. Patient recovered.

Rituxan Side Effects Report #5309497-6
Physician from UNITED STATES reported RITUXAN problem on Jan 11, 2005. Female patient, 43 years of age, weighting 188.1 lb, was diagnosed with systemic lupus erythematosus and was treated with RITUXAN. After drug was administered, patient experienced the following problems/side effects: activated partial thromboplastin time prolonged, antiphospholipid syndrome, condition aggravated, fibrin d dimer increased, leukopenia, meningitis, pancreatitis acute, pulmonary embolism, systemic lupus erythematosus, . RITUXAN dosage: unknown. During the same period patient was treated with METOPROLOL TARTRATE, FOLATE, MAXZIDE, GLYBURIDE, PREDNISONE, LISINOPRIL. Patient was hospitalized. Patient recovered.

Ortho Side Effects Report #5257772-6
ORTHO EVRA problem was reported by a Health Professional from UNITED STATES on Feb 28, 2007. Female patient, weighting 185.0 lb, was diagnosed with contraception and was treated with ORTHO EVRA. After drug was administered, patient experienced the following problems/side effects: anaemia, antiphospholipid syndrome, hepatic haematoma, mesenteric vein thrombosis, oesophageal varices haemorrhage, portal hypertension, portal vein thrombosis, pulmonary embolism, pulmonary hypertension, . ORTHO EVRA dosage: unknown. During the same period patient was treated with EXCEDRIN. Patient was hospitalized. Patient died on 07/06/2004.

Propylthiouracil Side Effects Report #5656237-7
Physician from JAPAN reported PROPYLTHIOURACIL problem on Feb 25, 2008. Female patient, 16 years of age, was diagnosed with basedow's disease and was treated with PROPYLTHIOURACIL. After drug was administered, patient experienced the following problems/side effects: abdominal pain upper, antineutrophil cytoplasmic antibody positive, antiphospholipid syndrome, arthralgia, cardiac murmur, coagulation factor xiii level decreased, deep vein thrombosis, glomerulonephritis, goitre, . PROPYLTHIOURACIL dosage: unknown. Patient was hospitalized. Patient recovered.

Fosamax Side Effects Report #5670868-X
FOSAMAX problem was reported by a Physician from UNITED STATES on Mar 04, 2008. Female patient, 36 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: abdominal pain, addison's disease, antiphospholipid syndrome, benign neoplasm, blood potassium decreased, bone density decreased, bronchitis, cerebellar atrophy, cerebellar infarction, . FOSAMAX dosage: unknown. During the same period patient was treated with PREDNISONE, NEURONTIN, PLAVIX, ASPIRIN, ADVAIR DISKUS, ALBUTEROL, MS CONTIN, TOPAMAX. Patient was hospitalized. Patient recovered.

Ovcon Side Effects Report #5679017-5
Consumer or non-health professional from UNITED STATES reported OVCON problem on Mar 11, 2008. Female patient, 21 years of age, weighting 147.9 lb, was diagnosed with ovarian cyst and was treated with OVCON. After drug was administered, patient experienced the following problems/side effects: alexia, antinuclear antibody positive, antiphospholipid syndrome, aortic valve incompetence, aphasia, blood pressure increased, cerebrovascular accident, convulsion, escherichia urinary tract infection, . OVCON dosage: unknown. Patient was hospitalized and became disabled. Patient recovered.

Fosamax Side Effects Report #5747857-X
FOSAMAX problem was reported by a Physician from UNITED STATES on May 14, 2008. Female patient, 36 years of age, was diagnosed with osteoporosis, systemic lupus erythematosus and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: abdominal pain, addison's disease, antiphospholipid syndrome, arthropathy, benign neoplasm, blood potassium decreased, bone density decreased, bronchitis, central nervous system lesion, . FOSAMAX dosage: unknown. During the same period patient was treated with PREDNISONE, NEURONTIN, PLAVIX, ASPIRIN, ADVAIR DISKUS, ALBUTEROL, MS CONTIN, TOPAMAX. Patient was hospitalized. Patient recovered.

Chlorpromazine Side Effects Report #5286833-0
Consumer or non-health professional from reported CHLORPROMAZINE problem on Mar 29, 2007. Female patient, 38 years of age, was diagnosed with schizoaffective disorder and was treated with CHLORPROMAZINE. After drug was administered, patient experienced the following problems/side effects: activated partial thromboplastin time prolonged, antiphospholipid antibodies, antiphospholipid syndrome, confusional state, grand mal convulsion, kaolin cephalin clotting time prolonged, russell's viper venom time abnormal, status epilepticus, thrombocytopenia, . CHLORPROMAZINE dosage: 100 MG/DAY. Patient was hospitalized. Patient recovered.

Ortho Side Effects Report #5291643-4
ORTHO EVRA problem was reported by a Health Professional from UNITED STATES on Apr 05, 2007. Female patient, weighting 185.0 lb, was diagnosed with contraception and was treated with ORTHO EVRA. After drug was administered, patient experienced the following problems/side effects: alanine aminotransferase increased, anaemia, antiphospholipid syndrome, aspartate aminotransferase increased, asthenia, atelectasis, cardio-respiratory arrest, cough, diarrhoea, . ORTHO EVRA dosage: unknown. During the same period patient was treated with EXCEDRIN. Patient was hospitalized. Patient died on 07/06/2004.