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Myfortic Side Effects Report #5649021-1
Health Professional from UNITED STATES reported MYFORTIC problem on Mar 03, 2008. Female patient, 56 years of age, weighting 145.0 lb, was diagnosed with renal transplant and was treated with MYFORTIC. After drug was administered, patient experienced the following problems/side effects: bone marrow disorder, bone marrow failure, . MYFORTIC dosage: unknown. Patient recovered.

Neulastim Side Effects Report #5626140-7
NEULASTIM problem was reported by a Physician from ISRAEL on Feb 01, 2008. Male patient, 30 years of age, was treated with NEULASTIM. After drug was administered, patient experienced the following problems/side effects: bone marrow disorder, bone pain, leukocytosis, osteonecrosis, . NEULASTIM dosage: unknown. During the same period patient was treated with CYCLOPHOSPHAMIDE, ADRIAMYCIN PFS, DOXORUBICIN HYDROCHLORIDE, ETOPOSIDE, PROCARBAZINE, DEXAMETHASONE, PREDNISONE, VINCRISTINE. Patient was hospitalized. Patient recovered.

Humira Side Effects Report #5565418-2
Consumer or non-health professional from UNITED KINGDOM reported HUMIRA problem on Dec 11, 2007. Male patient, weighting 216.1 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: bone marrow disorder, . HUMIRA dosage: unknown. During the same period patient was treated with BISOPROLOL, DIGOXIN, FINASTERIDE, INSULIN, LANSOPRAZOLE, LORATADINE, PERINDOPRIL, DICLOFENAC. Patient recovered.

Remicade Side Effects Report #5566552-3
REMICADE problem was reported by a Physician from UNITED KINGDOM on Dec 11, 2007. Male patient, weighting 216.1 lb, was diagnosed with rheumatoid arthritis and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: bone marrow disorder, . REMICADE dosage: unknown. During the same period patient was treated with BISOPROLOL, DIGOXIN, DOXAZOSIN MESYLATE, FINASTERIDE, FRUSEMIDE, GLUCOSAMINE, INSULIN, LANSOPRAZOLE. Patient recovered.


Prograf Side Effects Report #5572503-8
Physician from JAPAN reported PROGRAF problem on Dec 04, 2007. Female patient, 74 years of age, was diagnosed with rheumatoid arthritis and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: bone marrow disorder, myelodysplastic syndrome, . PROGRAF dosage: 1 MG, ORAL. During the same period patient was treated with RHEUMATREX. Patient was hospitalized. Patient recovered.

Avonex Side Effects Report #5574028-2
AVONEX problem was reported by a Physician from GERMANY on Dec 12, 2007. Female patient, 44 years of age, was diagnosed with relapsing-remitting multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: bone marrow disorder, chondrosis, spinal osteoarthritis, . AVONEX dosage: unknown. During the same period patient was treated with EUTHYROX, IBUPROFEN. Patient recovered.

Cellcept Side Effects Report #5507564-5
Physician from JAPAN reported CELLCEPT problem on Oct 25, 2007. Male patient, 23 years of age, weighting 112.4 lb, was treated with CELLCEPT. After drug was administered, patient experienced the following problems/side effects: bone marrow disorder, epstein-barr virus infection, gastrointestinal haemorrhage, histiocytosis haematophagic, multi-organ failure, sepsis, small intestine ulcer, . CELLCEPT dosage: unknown. During the same period patient was treated with PROGRAF, SIMULECT, BREDININ. Patient died on 12/26/2003.

Avonex Side Effects Report #5519387-1
AVONEX problem was reported by a Physician from GERMANY on Nov 06, 2007. Female patient, 44 years of age, was diagnosed with relapsing-remitting multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: bone marrow disorder, bone marrow tumour cell infiltration, chondropathy, spinal osteoarthritis, . AVONEX dosage: unknown. During the same period patient was treated with EUTHYROX, IBUPROFEN. Patient recovered.

Myfortic Side Effects Report #5524512-2
Physician from SPAIN reported MYFORTIC VS MMF problem on Nov 21, 2007. Male patient, 51 years of age, weighting 171.1 lb, was diagnosed with renal transplant and was treated with MYFORTIC VS MMF. After drug was administered, patient experienced the following problems/side effects: bone marrow disorder, haemolytic anaemia, leukopenia, myelodysplastic syndrome, pancytopenia, pyrexia, spleen operation, . MYFORTIC VS MMF dosage: 720 MG/DAILY. During the same period patient was treated with VALCYTE, PREDNISONE. Patient was hospitalized. Patient recovered.


Mycophenolic Side Effects Report #5476031-X
MYCOPHENOLIC ACID problem was reported by a Physician from SPAIN on Sept 26, 2007. Male patient, 51 years of age, weighting 171.1 lb, was diagnosed with renal transplant and was treated with MYCOPHENOLIC ACID. After drug was administered, patient experienced the following problems/side effects: bone marrow disorder, haemolytic anaemia, leukopenia, myelodysplastic syndrome, pancytopenia, pyrexia, . MYCOPHENOLIC ACID dosage: 720 MG/DAILY. During the same period patient was treated with VALCYTE, PREDNISONE. Patient was hospitalized. Patient recovered.

Rituxan Side Effects Report #5479956-4
Physician from HUNGARY reported RITUXAN problem on Oct 03, 2007. Female patient, weighting 127.9 lb, was diagnosed with mantle cell lymphoma and was treated with RITUXAN. After drug was administered, patient experienced the following problems/side effects: bone marrow disorder, febrile neutropenia, pneumonia, . RITUXAN dosage: 600 MG, Q3W. During the same period patient was treated with CYCLOPHOSPHAMIDE, EPIRUBICIN HYDROCHLORIDE. Patient was hospitalized. Patient recovered.

Rituxan Side Effects Report #5487256-1
RITUXAN problem was reported by a Physician from HUNGARY on Oct 03, 2007. Female patient, weighting 127.9 lb, was diagnosed with mantle cell lymphoma and was treated with RITUXAN. After drug was administered, patient experienced the following problems/side effects: bone marrow disorder, febrile neutropenia, pneumonia, . RITUXAN dosage: 600 MG, Q3W. During the same period patient was treated with CYCLOPHOSPHAMIDE, EPIRUBICIN HYDROCHLORIDE. Patient was hospitalized. Patient recovered.

Forteo Side Effects Report #5490755-X
Consumer or non-health professional from GERMANY reported FORTEO problem on Oct 08, 2007. Male patient was diagnosed with osteoporosis and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: bone marrow disorder, . FORTEO dosage: unknown. During the same period patient was treated with CORTISONE ACETATE, ANALGESICS. Patient recovered.

Remicade Side Effects Report #5502826-X
REMICADE problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Oct 22, 2007. Male patient, 78 years of age, weighting 182.0 lb, was diagnosed with rheumatoid arthritis and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: bone marrow disorder, eczema, gout, . REMICADE dosage: unknown. Patient was hospitalized. Patient recovered.


Daunorubicin Side Effects Report #5503120-3
Consumer or non-health professional from UNITED STATES reported DAUNORUBICIN problem on Oct 29, 2007. Male patient, weighting 269.8 lb, was treated with DAUNORUBICIN. After drug was administered, patient experienced the following problems/side effects: bone marrow disorder, deep vein thrombosis, . DAUNORUBICIN dosage: 108 MG. Patient was hospitalized. Patient recovered.

Avonex Side Effects Report #5451082-X
AVONEX problem was reported by a Physician from GERMANY on Sept 05, 2007. Female patient, 44 years of age, was diagnosed with relapsing-remitting multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: bone marrow disorder, chondropathy, . AVONEX dosage: unknown. Patient recovered.

Gleevec Side Effects Report #5401107-2
Physician from UNITED STATES reported GLEEVEC problem on July 23, 2007. Female patient, 70 years of age, was diagnosed with chronic myeloid leukaemia and was treated with GLEEVEC. After drug was administered, patient experienced the following problems/side effects: bone marrow disorder, chronic lymphocytic leukaemia, . GLEEVEC dosage: 400 MG, QD. Patient recovered.

Gleevec Side Effects Report #5401107-2
GLEEVEC problem was reported by a Physician from UNITED STATES on July 23, 2007. Female patient, 70 years of age, was diagnosed with chronic myeloid leukaemia and was treated with GLEEVEC. After drug was administered, patient experienced the following problems/side effects: bone marrow disorder, chronic lymphocytic leukaemia, . GLEEVEC dosage: 400 MG, QD. Patient recovered.

Thalomid Side Effects Report #5771371-9
Consumer or non-health professional from UNITED STATES reported THALOMID problem on June 02, 2008. Male patient, 86 years of age, was diagnosed with multiple myeloma and was treated with THALOMID. After drug was administered, patient experienced the following problems/side effects: bone marrow disorder, neoplasm malignant, prostate cancer, . THALOMID dosage: 50 MG, 1 IN 1 D, ORAL. Patient died on 05/31/2008.


Niaspan Side Effects Report #5774628-0
NIASPAN problem was reported by a Health Professional from GERMANY on June 04, 2008. Male patient, weighting 180.8 lb, was diagnosed with prophylaxis, tachycardia, diabetes mellitus and was treated with NIASPAN. After drug was administered, patient experienced the following problems/side effects: bone marrow disorder, gingival bleeding, platelet count decreased, pyrexia, red blood cell count decreased, white blood cell count decreased, . NIASPAN dosage: unknown. During the same period patient was treated with ACETYLSALICYLATE LYSINE, SOTALOL, ATORVASTATIN CALCIUM, GLICLAZIDE. Patient was hospitalized. Patient recovered.

Cerezyme Side Effects Report #5792078-8
Physician from NETHERLANDS reported CEREZYME problem on June 06, 2008. Male patient was diagnosed with gaucher's disease and was treated with CEREZYME. After drug was administered, patient experienced the following problems/side effects: bone marrow disorder, bone pain, osteonecrosis, . CEREZYME dosage: unknown. Patient was hospitalized. Patient recovered.

Cerezyme Side Effects Report #5792658-X
CEREZYME problem was reported by a Physician from NETHERLANDS on June 06, 2008. Male patient was diagnosed with gaucher's disease and was treated with CEREZYME. After drug was administered, patient experienced the following problems/side effects: bone marrow disorder, osteonecrosis, . CEREZYME dosage: unknown. Patient was hospitalized. Patient recovered.

Cerezyme Side Effects Report #5796032-1
Physician from UNITED STATES reported CEREZYME problem on June 23, 2008. Male patient, 47 years of age, weighting 145.5 lb, was diagnosed with gaucher's disease and was treated with CEREZYME. After drug was administered, patient experienced the following problems/side effects: bone marrow disorder, disease progression, gaucher's disease, hepatic cirrhosis, hepatitis c, hepatosplenomegaly, platelet count decreased, . CEREZYME dosage: unknown. Patient recovered.

Lyrica Side Effects Report #5735496-6
LYRICA problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 30, 2008. Male patient, weighting 172.0 lb, was diagnosed with musculoskeletal pain, perineal pain, neuralgia, hypertension, glaucoma and was treated with LYRICA. After drug was administered, patient experienced the following problems/side effects: bone marrow disorder, emphysema, haematocrit decreased, haemoglobin decreased, mean cell volume increased, monocyte count increased, somnolence, unevaluable event, . LYRICA dosage: unknown. During the same period patient was treated with AMBIEN, AMOXAPINE, SEROQUEL, LOTREL, TAMSULOSIN, XALATAN. Patient recovered.

Leustatin Side Effects Report #5735774-0
Physician from GERMANY reported LEUSTATIN problem on May 05, 2008. Male patient, child 5 years of age, was diagnosed with malignant histiocytosis and was treated with LEUSTATIN. After drug was administered, patient experienced the following problems/side effects: bone marrow disorder, neutrophil count decreased, white blood cell count decreased, . LEUSTATIN dosage: unknown. Patient recovered.

Avastin Side Effects Report #5745191-5
AVASTIN problem was reported by a Physician from UNITED KINGDOM on May 06, 2008. Female patient, 47 years of age, weighting 143.3 lb, was diagnosed with breast cancer and was treated with AVASTIN. After drug was administered, patient experienced the following problems/side effects: bone marrow disorder, epistaxis, gastrointestinal haemorrhage, thrombocytopenia, . AVASTIN dosage: 20 MG/KG, UNK. Patient recovered.

Bevacizumab Side Effects Report #5745899-1
Consumer or non-health professional from UNITED KINGDOM reported BEVACIZUMAB problem on May 06, 2008. Male patient, weighting 160.9 lb, was diagnosed with colorectal cancer metastatic and was treated with BEVACIZUMAB. After drug was administered, patient experienced the following problems/side effects: bone marrow disorder, . BEVACIZUMAB dosage: 365 MG, 2/WEEK. During the same period patient was treated with FLUOROURACIL, IRINOTECAN. Patient was hospitalized. Patient recovered.

Leustatin Side Effects Report #5746606-9
LEUSTATIN problem was reported by a Physician from GERMANY on May 13, 2008. Male patient, child 5 years of age, was diagnosed with malignant histiocytosis and was treated with LEUSTATIN. After drug was administered, patient experienced the following problems/side effects: bone marrow disorder, neutrophil count decreased, white blood cell count decreased, . LEUSTATIN dosage: unknown. Patient recovered.

Bevacizumab Side Effects Report #5750054-5
Consumer or non-health professional from UNITED KINGDOM reported BEVACIZUMAB problem on May 15, 2008. Male patient, weighting 160.9 lb, was diagnosed with colorectal cancer metastatic and was treated with BEVACIZUMAB. After drug was administered, patient experienced the following problems/side effects: bone marrow disorder, . BEVACIZUMAB dosage: 365 MG, 2/WEEK. During the same period patient was treated with FLUOROURACIL, IRINOTECAN. Patient was hospitalized. Patient recovered.

Leustatin Side Effects Report #5753721-2
LEUSTATIN problem was reported by a Physician from GERMANY on May 26, 2008. Male patient, weighting 41.45 lb, was diagnosed with malignant histiocytosis, infection prophylaxis, epilepsy and was treated with LEUSTATIN. After drug was administered, patient experienced the following problems/side effects: bone marrow disorder, pancytopenia, . LEUSTATIN dosage: unknown. During the same period patient was treated with TRIMETHOPRIM, AMPHOTERICIN B, VALPROATE, SULFAMETHOXAZOL. Patient was hospitalized. Patient recovered.

Niaspan Side Effects Report #5695147-6
Health Professional from GERMANY reported NIASPAN problem on Mar 17, 2008. Male patient, 63 years of age, was treated with NIASPAN. After drug was administered, patient experienced the following problems/side effects: bone marrow disorder, gingival bleeding, platelet count decreased, pyrexia, . NIASPAN dosage: unknown. During the same period patient was treated with SOTALOL, ATORVASTATIN CALCIUM, GLICLAZIDE. Patient was hospitalized. Patient recovered.

Remicade Side Effects Report #5695893-4
REMICADE problem was reported by a Physician from GERMANY on Mar 27, 2008. Female patient, 41 years of age, weighting 116.8 lb, was diagnosed with colitis ulcerative and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: bone marrow disorder, meningitis listeria, pancytopenia, photosensitivity reaction, . REMICADE dosage: unknown. During the same period patient was treated with METHOTREXATE, PREDNISOLONE. Patient was hospitalized. Patient recovered.

Imatinib Side Effects Report #5703664-5
Health Professional from ISRAEL reported IMATINIB problem on Mar 31, 2008. Male patient, 57 years of age, was treated with IMATINIB. After drug was administered, patient experienced the following problems/side effects: bone marrow disorder, bone marrow harvest failure, pancytopenia, . IMATINIB dosage: 400 MG, QD. Patient recovered.

Imatinib Side Effects Report #5703704-3
IMATINIB problem was reported by a Health Professional from ISRAEL on Mar 31, 2008. Female patient, 23 years of age, was diagnosed with chronic myeloid leukaemia and was treated with IMATINIB. After drug was administered, patient experienced the following problems/side effects: bone marrow disorder, bone marrow failure, bone marrow harvest failure, . IMATINIB dosage: 400 MG/D. Patient recovered.

Raptiva Side Effects Report #5707365-9
Physician from UNITED STATES reported RAPTIVA problem on Apr 04, 2008. Female patient, 54 years of age, was diagnosed with psoriasis and was treated with RAPTIVA. After drug was administered, patient experienced the following problems/side effects: bone marrow disorder, hepatocellular injury, intestinal obstruction, myocardial infarction, pulmonary oedema, renal failure, . RAPTIVA dosage: 72 MG, 1/WEEK. During the same period patient was treated with DARVOCET. Patient was hospitalized. Patient died on 12/27/2007.

Fludarabine Side Effects Report #5723832-6
FLUDARABINE PHOSPHATE problem was reported by a Health Professional from UNITED STATES on Apr 29, 2008. Male patient, weighting 143.3 lb, was diagnosed with myelodysplastic syndrome and was treated with FLUDARABINE PHOSPHATE. After drug was administered, patient experienced the following problems/side effects: bone marrow disorder, cardiac tamponade, continuous haemodiafiltration, hypotension, pancytopenia, pericardial effusion, pulmonary oedema, pyrexia, renal failure, . FLUDARABINE PHOSPHATE dosage: 30MG/M2 DAILY IV DRIP. During the same period patient was treated with THIOTEPA, TOTAL BODY IRRADIATION, RABBIT ATG. Patient died on 04/26/2008.

Zevalin Side Effects Report #5336458-3
Health Professional from UNITED STATES reported ZEVALIN problem on May 14, 2007. Female patient was treated with ZEVALIN. After drug was administered, patient experienced the following problems/side effects: bone marrow disorder, . ZEVALIN dosage: unknown. During the same period patient was treated with RITUXIMAB. Patient recovered.

Valsartan Side Effects Report #5295897-X
VALSARTAN problem was reported by a Physician from UNITED KINGDOM on Apr 02, 2007. Male patient, weighting 228.6 lb, was diagnosed with glucose tolerance impaired and was treated with VALSARTAN. After drug was administered, patient experienced the following problems/side effects: bone marrow disorder, chest wall mass, erythema, follicle centre lymphoma, follicular grade i, ii, iii stage iv, lymphadenopathy, lymphocyte count increased, mass excision, neoplasm malignant, neoplasm progression, . VALSARTAN dosage: unknown. During the same period patient was treated with ATORVASTATIN CALCIUM, BENDROFLUAZIDE, AMLODIPINE, BISOPRODOL FUMARATE, ASPIRIN, NITROGLYCERIN, NATEGLINIDE. Patient recovered.

Amiodarone Side Effects Report #5305009-1
Physician from UNITED STATES reported AMIODARONE problem on Apr 04, 2007. Male patient, 81 years of age, was diagnosed with atrial fibrillation and was treated with AMIODARONE. After drug was administered, patient experienced the following problems/side effects: bone marrow disorder, granuloma, hepatic cirrhosis, hepatomegaly, hyperthyroidism, leukopenia, neutrophil pelger-huet anomaly present, spleen palpable, splenomegaly, . AMIODARONE dosage: unknown. Patient recovered.

Lamisil Side Effects Report #5252906-1
LAMISIL problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 19, 2007. Female patient, child 8 years of age, was diagnosed with nail tinea and was treated with LAMISIL. After drug was administered, patient experienced the following problems/side effects: bone marrow disorder, white blood cell count decreased, . LAMISIL dosage: 250 MG, QD. Patient recovered.

Betaseron Side Effects Report #5258084-7
Physician from UNITED STATES reported BETASERON problem on Feb 23, 2007. Female patient, 38 years of age, weighting 135.0 lb, was diagnosed with relapsing-remitting multiple sclerosis and was treated with BETASERON. After drug was administered, patient experienced the following problems/side effects: bone marrow disorder, choking sensation, hypoaesthesia, livedo reticularis, migraine, pain, systemic lupus erythematosus, thyroid disorder, . BETASERON dosage: unknown. During the same period patient was treated with VESACARE, ADDERALL, CELEXA, BACLOFEN, TIZANIDINE, AMANTADINE. Patient recovered.

Avonex Side Effects Report #5262649-6
AVONEX problem was reported by a Consumer or non-health professional from GERMANY on Feb 20, 2007. Female patient, 50 years of age, weighting 264.6 lb, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: bone marrow disorder, breast cancer, influenza like illness, metastases to bone, oestrogen receptor assay positive, plasmacytoma, progesterone receptor assay positive, pyrexia, rib fracture, . AVONEX dosage: unknown. During the same period patient was treated with VALSARTAN AND HYDROCHLOROTHIAZIDE. Patient was hospitalized. Patient recovered.

Mylotarg Side Effects Report #5277365-4
Physician from UNITED STATES reported MYLOTARG problem on Mar 15, 2007. Male patient, 75 years of age, was diagnosed with acute myeloid leukaemia and was treated with MYLOTARG. After drug was administered, patient experienced the following problems/side effects: bone marrow disorder, granuloma, liver disorder, . MYLOTARG dosage: 9 MG/M^2. Patient recovered.

Isentress Side Effects Report #5649950-9
ISENTRESS problem was reported by a Physician from UNITED STATES on Feb 28, 2008. Female patient, 39 years of age, was diagnosed with hiv infection and was treated with ISENTRESS. After drug was administered, patient experienced the following problems/side effects: anaemia, bone marrow disorder, thrombocytopenia, . ISENTRESS dosage: unknown. During the same period patient was treated with FUZEON, NORVIR, TRUVADA, BIAXIN. Patient died on 02/09/2008.

Isentress Side Effects Report #5662297-X
Physician from UNITED STATES reported ISENTRESS problem on Mar 04, 2008. Female patient, 39 years of age, was diagnosed with hiv infection and was treated with ISENTRESS. After drug was administered, patient experienced the following problems/side effects: anaemia, bone marrow disorder, rectal haemorrhage, thrombocytopenia, . ISENTRESS dosage: unknown. During the same period patient was treated with FUZEON, NORVIR, TRUVADA, BIAXIN. Patient died on 02/09/2008.

Isentress Side Effects Report #5684434-3
ISENTRESS problem was reported by a Physician from UNITED STATES on Mar 24, 2008. Female patient, 39 years of age, weighting 79.37 lb, was diagnosed with hiv infection, mycobacteria test, antifungal prophylaxis and was treated with ISENTRESS. After drug was administered, patient experienced the following problems/side effects: anaemia, bone marrow disorder, thrombocytopenia, . ISENTRESS dosage: unknown. During the same period patient was treated with FUZEON, NORVIR, TRUVADA, BIAXIN, BACTRIM DS, BACTRIM DS. Patient was hospitalized and became disabled. Patient died on 02/09/2008.

Vidaza Side Effects Report #5643881-6
Health Professional from UNITED STATES reported VIDAZA problem on Feb 14, 2008. Male patient, 65 years of age, weighting 176.4 lb, was diagnosed with myeloproliferative disorder and was treated with VIDAZA. After drug was administered, patient experienced the following problems/side effects: abdominal pain, bone marrow disorder, cerebrovascular accident, musculoskeletal pain, necrosis, rash erythematous, respiratory disorder, splenic infarction, . VIDAZA dosage: 75 MG/M2,DAILY X 5 DAYS , INTRAVENOUS. During the same period patient was treated with PROCHLORPERAZINE MALEATE, DOCUSATE, SENNA, FIBERCON, BENADRYL, ACETAMINOPHEN. Patient was hospitalized. Patient recovered.

Fosamax Side Effects Report #5585618-5
FOSAMAX problem was reported by a Pharmacist from UNITED STATES on Jan 04, 2008. Female patient, 57 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: bone disorder, bone marrow disorder, bone pain, impaired healing, . FOSAMAX dosage: unknown. During the same period patient was treated with ESTRACE, VIVELLE, LUNESTA, LORTAB, FIORICET. Patient recovered.

Remicade Side Effects Report #5586532-1
Physician from UNITED KINGDOM reported REMICADE problem on Jan 04, 2008. Male patient, weighting 216.1 lb, was diagnosed with rheumatoid arthritis and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: anaemia, bone marrow disorder, cardiac failure congestive, renal failure, . REMICADE dosage: unknown. During the same period patient was treated with BISOPROLOL, DIGOXIN, DOXAZOSIN, FINASTERIDE, FUROSEMIDE, GLUCOSAMINE, INSULIN, LANSOPRAZOLE. Patient was hospitalized. Patient recovered.

Rebif Side Effects Report #5548426-7
REBIF problem was reported by a Consumer or non-health professional from BRAZIL on Nov 22, 2007. Female patient, 49 years of age, was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: asthenia, bone marrow disorder, gait disturbance, lipoma, multiple sclerosis relapse, nuclear magnetic resonance imaging abnormal, . REBIF dosage: unknown. Patient was hospitalized and became disabled. 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.