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Remicade Side Effects Report #5598643-5
Physician from UNITED STATES reported REMICADE problem on Jan 16, 2008. Male patient, 55 years of age, was diagnosed with psoriatic arthropathy and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: blood immunoglobulin a increased, blood testosterone decreased, pyoderma gangrenosum, vitiligo, . REMICADE dosage: unknown. During the same period patient was treated with PLETAL, DAYPRO, CORTICOSTEROIDS. Patient recovered.

Revlimid Side Effects Report #5638573-3
REVLIMID problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 13, 2007. Male patient was diagnosed with multiple myeloma and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: blood immunoglobulin a increased, . REVLIMID dosage: 25 MG, QD, ORAL. Patient recovered.

Escitalopram Side Effects Report #5550953-3
Consumer or non-health professional from FRANCE reported ESCITALOPRAM problem on Nov 23, 2007. Female patient, 64 years of age, was treated with ESCITALOPRAM. After drug was administered, patient experienced the following problems/side effects: blood immunoglobulin a increased, leukocytoclastic vasculitis, . ESCITALOPRAM dosage: unknown. During the same period patient was treated with OXAZEPAM, ZOLPIDEM TARTRATE, DIAMICRON, TENSTATEN, BISOPROLOL FUMARATE, THERALENE. Patient was hospitalized. Patient recovered.

Furadantin Side Effects Report #5552121-8
FURADANTIN problem was reported by a Physician from FRANCE on Nov 26, 2007. Female patient, 81 years of age, was treated with FURADANTIN. After drug was administered, patient experienced the following problems/side effects: blood immunoglobulin a increased, blood immunoglobulin e increased, blood immunoglobulin g increased, blood immunoglobulin m increased, leukocytoclastic vasculitis, . FURADANTIN dosage: unknown. During the same period patient was treated with INEXIUM, TOPAAL, BACTRIM, LERCANIDIPINE. Patient was hospitalized. Patient recovered.


Velcade Side Effects Report #5580110-6
Physician from PORTUGAL reported VELCADE problem on Dec 17, 2007. Female patient, child 1 years of age, was diagnosed with multiple myeloma and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: blood immunoglobulin a increased, neuropathy, no therapeutic response, urinary tract infection, urinary tract obstruction, . VELCADE dosage: 1.00 MG/M2. Patient recovered.

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

Velcade Side Effects Report #5701453-9
Physician from SPAIN reported VELCADE problem on Mar 24, 2008. Male patient, 57 years of age, weighting 147.7 lb, was diagnosed with multiple myeloma and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: blood immunoglobulin a increased, candidiasis, cardiac failure congestive, disease progression, haemodialysis, hypercalcaemia, lung infiltration, multi-organ failure, pneumonia, . VELCADE dosage: 1.3 MG/M2. During the same period patient was treated with DEXAMETHASONE, PAMIDRONATE DI, DUROGESIN, NEORECORMON, SEPTRINTE, ACYCLOVIR, VENTOLIN, CLINDAMYCIN. Patient was hospitalized. Patient died on 07/11/2007.

Thalidomide Side Effects Report #5357212-2
THALIDOMIDE problem was reported by a Physician from UNITED KINGDOM on May 31, 2007. Male patient, 74 years of age, was diagnosed with leukaemia plasmacytic and was treated with THALIDOMIDE. After drug was administered, patient experienced the following problems/side effects: blood immunoglobulin a increased, condition aggravated, disease progression, polyneuropathy, pulmonary hypertension, . THALIDOMIDE dosage: 50 MG, 1 IN 1 D, ORAL. During the same period patient was treated with VELCADE, VINCRISTINE, BENDAMUSTIN, DEXAMETHASONE, ADRIAMYCIN PFS, LYRICA. Patient was hospitalized. Patient recovered.

Revlimid Side Effects Report #5333494-8
Pharmacist from UNITED STATES reported REVLIMID problem on May 22, 2007. Male patient was diagnosed with multiple myeloma and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: blood immunoglobulin a increased, febrile neutropenia, . REVLIMID dosage: 25MG DAILY 21D/28D PO. During the same period patient was treated with MAXZIDE, MEGESTROL ACETATE, FAMOTIDINE, FLUOXETINE, PROCRIT, PROVENTIL, NEUPOGEN, PROMETHAZINE. Patient recovered.


Avonex Side Effects Report #5264128-9
AVONEX problem was reported by a Physician 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: blood immunoglobulin a increased, blood uric acid increased, bone marrow disorder, bone pain, breast cancer metastatic, haemoglobin decreased, influenza like illness, lymphadenopathy, mean cell volume decreased, . AVONEX dosage: unknown. During the same period patient was treated with VALSARTAN AND HYDROCHLOROTHIAZIDE. Patient was hospitalized. Patient recovered.

Velcade Side Effects Report #5268352-0
Consumer or non-health professional from UNITED STATES reported VELCADE problem on Mar 14, 2007. Female patient, weighting 177.5 lb, was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: blood immunoglobulin a increased, bone pain, condition aggravated, disease progression, dyspnoea, liver function test abnormal, oedema peripheral, pitting oedema, refusal of treatment by patient, . VELCADE dosage: 6.4 MG. During the same period patient was treated with THALOMID, DEXAMETHASONE. Patient was hospitalized. Patient recovered.

Exjade Side Effects Report #5524753-4
EXJADE problem was reported by a Physician from GERMANY on Nov 19, 2007. Female patient, 17 years of age, was diagnosed with haemosiderosis and was treated with EXJADE. After drug was administered, patient experienced the following problems/side effects: antibody test positive, blood immunoglobulin a increased, blood immunoglobulin g increased, campylobacter infection, diplopia, guillain-barre syndrome, ivth nerve paresis, monoparesis, quadriplegia, . EXJADE dosage: 1750 MG, QD. During the same period patient was treated with ROCALTROL, CYCLO. Patient was hospitalized. Patient recovered.

Remicade Side Effects Report #5737084-4
Physician from UNITED STATES reported REMICADE problem on May 06, 2008. Male patient, 55 years of age, was diagnosed with psoriatic arthropathy and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: antinuclear antibody, blood immunoglobulin a increased, blood testosterone decreased, pyoderma gangrenosum, thyroiditis, vitiligo, . REMICADE dosage: unknown. During the same period patient was treated with PLETAL, DAYPRO, CORTICOSTEROIDS. Patient recovered.

Terbinafine Side Effects Report #5363268-3
TERBINAFINE problem was reported by a Physician from UNITED STATES on June 18, 2007. Male patient, 57 years of age, was treated with TERBINAFINE. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, blood immunoglobulin a increased, blood immunoglobulin g increased, chronic hepatitis, contusion, hepatic cirrhosis, hepatic necrosis, hepatitis b, hepatomegaly, . TERBINAFINE dosage: unknown. Patient recovered.


Cyclosporine Side Effects Report #5491547-8
Consumer or non-health professional from UNITED STATES reported CYCLOSPORINE problem on Oct 12, 2007. Female patient, child 3 years of age, was diagnosed with bone marrow transplant, immunosuppression, hypertension and was treated with CYCLOSPORINE. After drug was administered, patient experienced the following problems/side effects: auricular swelling, bacterial sepsis, blood immunoglobulin a increased, bone marrow disorder, dermatitis, helicobacter infection, hypertension, . CYCLOSPORINE dosage: unknown. During the same period patient was treated with PREDNISOLONE, ENALAPRIL MALEATE, ENALAPRIL MALEATE, AMLODIPINE. Patient was hospitalized. Patient recovered.

Thalidomide Side Effects Report #5397244-1
THALIDOMIDE problem was reported by a Physician from UNITED KINGDOM on July 12, 2007. Male patient, 74 years of age, was diagnosed with leukaemia plasmacytic and was treated with THALIDOMIDE. After drug was administered, patient experienced the following problems/side effects: angiocentric lymphoma, biopsy bone marrow abnormal, blood immunoglobulin a increased, blood lactate dehydrogenase increased, blood viscosity increased, cardiomegaly, chest discomfort, chest x-ray abnormal, condition aggravated, . THALIDOMIDE dosage: 50 MG, 1 IN 1 D, ORAL. During the same period patient was treated with VELCADE, VINCRISTINE, BENDAMUSTIN, ADRIAMYCIN PFS, PLAVIX, METOPROLOL SUCCINATE. Patient was hospitalized. Patient died on 06/14/2007.

Thalidomide Side Effects Report #5397244-1
Physician from UNITED KINGDOM reported THALIDOMIDE problem on July 12, 2007. Male patient, 74 years of age, was diagnosed with leukaemia plasmacytic and was treated with THALIDOMIDE. After drug was administered, patient experienced the following problems/side effects: angiocentric lymphoma, biopsy bone marrow abnormal, blood immunoglobulin a increased, blood lactate dehydrogenase increased, blood viscosity increased, cardiomegaly, chest discomfort, chest x-ray abnormal, condition aggravated, . THALIDOMIDE dosage: 50 MG, 1 IN 1 D, ORAL. During the same period patient was treated with VELCADE, VINCRISTINE, BENDAMUSTIN, ADRIAMYCIN PFS, PLAVIX, METOPROLOL SUCCINATE. Patient was hospitalized. Patient died on 06/14/2007.

Velcade Side Effects Report #5706344-5
VELCADE problem was reported by a Physician from JAPAN on Apr 02, 2008. Male patient, 54 years of age, weighting 132.3 lb, was diagnosed with multiple myeloma and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: blood chloride decreased, blood glucose increased, blood immunoglobulin a increased, condition aggravated, disease recurrence, graft versus host disease, haemorrhagic diathesis, hepatic function abnormal, herpes zoster, . VELCADE dosage: 2.20 MG, INTRAVENOUS. During the same period patient was treated with DECADRON, DEXAMETHASONE, URINORM, RABEPRAZOLE, ITRACONAZOLE, PROGRAF, LEVOFLOXACIN, SULFAMETHOXAZOLE AND TRIMETHOPRIM. Patient was hospitalized. Patient recovered.

Zometa Side Effects Report #5319832-0
Consumer or non-health professional from GERMANY reported ZOMETA problem on Apr 30, 2007. Female patient, 75 years of age, was diagnosed with osteopenia, plasmacytoma and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: actinomycosis, blood creatinine increased, blood immunoglobulin a increased, bone disorder, condition aggravated, dental alveolar anomaly, dental fistula, dental operation, . ZOMETA dosage: unknown. During the same period patient was treated with ACETYLSALICYLIC ACID SRT, ALKERAN, FORTECORTIN. Patient was hospitalized. Patient recovered.


Avonex Side Effects Report #5324647-3
AVONEX problem was reported by a Consumer or non-health professional from GERMANY on Apr 23, 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: adenoid cystic carcinoma, beta 2 microglobulin increased, blood immunoglobulin a increased, blood uric acid increased, bone cancer metastatic, bone marrow disorder, bone pain, breast cancer female, haemoglobin decreased, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.

Isoniazid Side Effects Report #5299697-6
Physician from JAPAN reported ISONIAZID problem on Mar 30, 2007. Male patient, 38 years of age, weighting 123.5 lb, was diagnosed with tuberculosis and was treated with ISONIAZID. After drug was administered, patient experienced the following problems/side effects: abdominal pain, arthralgia, blood immunoglobulin a increased, glomerulonephritis proliferative, henoch-schonlein purpura, leukocytoclastic vasculitis, proteinuria, pyrexia, . ISONIAZID dosage: 300 MG. During the same period patient was treated with RIFAMPICIN, ETHAMBUTOL HYDROCHLORIDE, PYRAZINAMIDE. Patient recovered.