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Tracleer Side Effects Report #5385888-2
Physician from GREECE reported TRACLEER problem on June 28, 2007. Male patient, 50 years of age, was diagnosed with pulmonary hypertension and was treated with TRACLEER. After drug was administered, patient experienced the following problems/side effects: haemosiderosis, hepatic neoplasm malignant, . TRACLEER dosage: 125 MG, ORAL. Patient recovered.

Tracleer Side Effects Report #5385888-2
TRACLEER problem was reported by a Physician from GREECE on June 28, 2007. Male patient, 50 years of age, was diagnosed with pulmonary hypertension and was treated with TRACLEER. After drug was administered, patient experienced the following problems/side effects: haemosiderosis, hepatic neoplasm malignant, . TRACLEER dosage: 125 MG, ORAL. Patient recovered.

Concerta Side Effects Report #5292952-5
Physician from SWEDEN reported CONCERTA problem on Mar 30, 2007. Male patient, 48 years of age, was diagnosed with attention deficit/hyperactivity disorder, arthralgia and was treated with CONCERTA. After drug was administered, patient experienced the following problems/side effects: haemosiderosis, lipomatosis, porphyria non-acute, . CONCERTA dosage: unknown. During the same period patient was treated with DICLOFENAC. Patient recovered.

Neulasta Side Effects Report #5387502-9
NEULASTA problem was reported by a Physician from PORTUGAL on July 06, 2007. Female patient, weighting 132.3 lb, was treated with NEULASTA. After drug was administered, patient experienced the following problems/side effects: bone marrow failure, haemosiderosis, no therapeutic response, . NEULASTA dosage: unknown. During the same period patient was treated with NEUPOGEN, FLUOROURACIL, DOXORUBICIN HYDROCHLORIDE, CYCLOPHOSPHAMIDE, ACECLOFENAC, THIOCHOLCHICOSIDE, NSAIDS. Patient was hospitalized. Patient recovered.


Neulasta Side Effects Report #5387502-9
Physician from PORTUGAL reported NEULASTA problem on July 06, 2007. Female patient, weighting 132.3 lb, was treated with NEULASTA. After drug was administered, patient experienced the following problems/side effects: bone marrow failure, haemosiderosis, no therapeutic response, . NEULASTA dosage: unknown. During the same period patient was treated with NEUPOGEN, FLUOROURACIL, DOXORUBICIN HYDROCHLORIDE, CYCLOPHOSPHAMIDE, ACECLOFENAC, THIOCHOLCHICOSIDE, NSAIDS. Patient was hospitalized. Patient recovered.

Decadron Side Effects Report #5301540-3
DECADRON problem was reported by a Consumer or non-health professional from JAPAN on Apr 02, 2007. Male patient, 21 years of age, was diagnosed with t-cell lymphoma recurrent and was treated with DECADRON. After drug was administered, patient experienced the following problems/side effects: decreased immune responsiveness, haemosiderosis, hepatitis e, hepatitis post transfusion, lymphopenia, pancytopenia, . DECADRON dosage: 40 MG/DAILY PO. During the same period patient was treated with INJ IFOMIDE, ETOPOSIDE, CYTARABINE, INJ UROMITEXAN. Patient died.

Velcade Side Effects Report #5679728-1
Physician from UNITED STATES reported VELCADE problem on Mar 13, 2008. Male patient, 65 years of age, weighting 208.1 lb, was diagnosed with multiple myeloma and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: bacterial infection, bronchopneumonia, haemosiderosis, . VELCADE dosage: 2.3 MG, INTRAVENOUS. During the same period patient was treated with REVLIMID, DEXAMETHASONE, LOPRESSOR, MEPRON, NORVASC, OMEPRAZOLE, OXYCODONE, THYROID. Patient was hospitalized. Patient died on 11/11/2007.

Busulfan Side Effects Report #5585753-1
BUSULFAN problem was reported by a Consumer or non-health professional from JAPAN on Dec 21, 2007. Male patient, child 7 years of age, was diagnosed with stem cell transplant and was treated with BUSULFAN. After drug was administered, patient experienced the following problems/side effects: coagulopathy, gastritis, haemosiderosis, hepatic function abnormal, hyperbilirubinaemia, hypoproteinaemia, neutropenia, pneumocystis jiroveci pneumonia, renal impairment, . BUSULFAN dosage: 6 ML; ; IV. Patient was hospitalized. Patient died.

Forteo Side Effects Report #5376880-2
Consumer or non-health professional from FRANCE reported FORTEO problem on June 20, 2007. Female patient, 52 years of age, was diagnosed with osteoporosis, haemosiderosis and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: cognitive disorder, fatigue, haemosiderosis, hearing impaired, motor dysfunction, visual acuity reduced, . FORTEO dosage: unknown. During the same period patient was treated with CORTISONE ACETATE, CORTISONE ACETATE. Patient was hospitalized. Patient recovered.


Forteo Side Effects Report #5376880-2
FORTEO problem was reported by a Consumer or non-health professional from FRANCE on June 20, 2007. Female patient, 52 years of age, was diagnosed with osteoporosis, haemosiderosis and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: cognitive disorder, fatigue, haemosiderosis, hearing impaired, motor dysfunction, visual acuity reduced, . FORTEO dosage: unknown. During the same period patient was treated with CORTISONE ACETATE, CORTISONE ACETATE. Patient was hospitalized. Patient recovered.

Actonel Side Effects Report #5278451-5
Physician from UNITED STATES reported ACTONEL problem on Mar 07, 2007. Female patient, 81 years of age, was diagnosed with osteoporosis postmenopausal and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: antinuclear antibody positive, granulomatous liver disease, haemosiderosis, hepatic steatosis, hepatitis, . ACTONEL dosage: unknown. During the same period patient was treated with FLUVASTATIN, METOPROLOL TARTRATE, ACETAMINOPHEN, ASPIRIN, CALCIUM CARBONATE. Patient recovered.