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BLOOD IMMUNOGLOBULIN M INCREASED side effect

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Zavesca Side Effects Report #5531508-3
Consumer or non-health professional from GREECE reported ZAVESCA problem on Nov 14, 2007. Female patient, 67 years of age, weighting 169.8 lb, was diagnosed with gaucher's disease and was treated with ZAVESCA. After drug was administered, patient experienced the following problems/side effects: blood immunoglobulin m increased, diarrhoea, hepatomegaly, pancytopenia, splenomegaly, tremor, vibration test abnormal, . ZAVESCA dosage: 100 MG, QD, ORAL; 100 MG, BID, ORAL; 100 MG, BID, ORAL. During the same period patient was treated with ALENDRONATE. Patient recovered.

Thalomid Side Effects Report #5412192-6
THALOMID problem was reported by a Physician from UNITED STATES on Aug 02, 2007. Male patient, 65 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 m increased, disease progression, hip fracture, interstitial lung disease, no therapeutic response, paraproteinaemia, . THALOMID dosage: unknown. During the same period patient was treated with ZANTAC, NAPROSYN, VELCADE, NORTRIPTYLINE, LIPITOR, LASIX, VITAMIN, CLONAZEPAM. Patient was hospitalized. Patient recovered.

Remicade Side Effects Report #5427179-7
Physician from UNITED STATES reported REMICADE problem on Aug 17, 2007. Male patient, child 11 years of age, was diagnosed with idiopathic thrombocytopenic purpura and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: blood immunoglobulin m increased, . REMICADE dosage: unknown. Patient recovered.

Copaxone Side Effects Report #5386004-3
COPAXONE problem was reported by a Consumer or non-health professional from GERMANY on June 27, 2007. Female patient, 30 years of age, was diagnosed with multiple sclerosis and was treated with COPAXONE. After drug was administered, patient experienced the following problems/side effects: blood immunoglobulin m increased, cell-mediated immune deficiency, herpes simplex, thrombocytopenia, vaginal candidiasis, . COPAXONE dosage: 20 MG (20 MG, 1 IN 1 D) SUBCUTANEOUS. Patient recovered.


Copaxone Side Effects Report #5386004-3
Consumer or non-health professional from GERMANY reported COPAXONE problem on June 27, 2007. Female patient, 30 years of age, was diagnosed with multiple sclerosis and was treated with COPAXONE. After drug was administered, patient experienced the following problems/side effects: blood immunoglobulin m increased, cell-mediated immune deficiency, herpes simplex, thrombocytopenia, vaginal candidiasis, . COPAXONE dosage: 20 MG (20 MG, 1 IN 1 D) SUBCUTANEOUS. Patient recovered.

Copaxone Side Effects Report #5369949-X
COPAXONE problem was reported by a Pharmacist from GERMANY on June 06, 2007. Female patient, 30 years of age, was diagnosed with multiple sclerosis and was treated with COPAXONE. After drug was administered, patient experienced the following problems/side effects: blood immunoglobulin m increased, cell-mediated immune deficiency, herpes zoster, idiopathic thrombocytopenic purpura, vaginal candidiasis, . COPAXONE dosage: 20 MG (20 MG, 1 IN 1 D); SUBCUTANEOUS. Patient recovered.

Leuprolide Side Effects Report #5580210-0
Consumer or non-health professional from FRANCE reported LEUPROLIDE ACETATE problem on Dec 26, 2007. Female patient, child 12 years of age, was diagnosed with growth retardation and was treated with LEUPROLIDE ACETATE. After drug was administered, patient experienced the following problems/side effects: abdominal pain, blood immunoglobulin m increased, confusional state, disorientation, dizziness, hallucination, visual, headache, hyperacusis, migraine, . LEUPROLIDE ACETATE dosage: 11.25 MG (11.25 MG, 1 IN 3M), SUBCUTANEOUS. During the same period patient was treated with SOMATROPIN. Patient was hospitalized. Patient recovered.

Mycophenolate Side Effects Report #5512744-9
MYCOPHENOLATE MOFETIL problem was reported by a Physician from ARGENTINA on Oct 31, 2007. Female patient, 16 years of age, weighting 132.3 lb, was diagnosed with lupus nephritis and was treated with MYCOPHENOLATE MOFETIL. After drug was administered, patient experienced the following problems/side effects: blood immunoglobulin g increased, blood immunoglobulin m increased, cardiomegaly, hypertension, infection, lupus nephritis, lymphadenopathy, odynophagia, oliguria, . MYCOPHENOLATE MOFETIL dosage: unknown. During the same period patient was treated with MYCOPHENOLATE MOFETIL, MYCOPHENOLATE MOFETIL, AZATHIOPRINE, METHYLPREDNISOLONE, CYCLOPHOSPHAMIDE, FUROSEMIDE. Patient was hospitalized and became disabled. Patient recovered.

Zometa Side Effects Report #5401136-9
Health Professional from GERMANY reported ZOMETA problem on July 23, 2007. Male patient, 60 years of age, was diagnosed with bone pain and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: actinomycosis, blood immunoglobulin m increased, bone debridement, bone disorder, bone pain, facial pain, fibrosis, impaired healing, neurolysis, . ZOMETA dosage: unknown. During the same period patient was treated with AREDIA. Patient recovered.


Zometa Side Effects Report #5401136-9
ZOMETA problem was reported by a Health Professional from GERMANY on July 23, 2007. Male patient, 60 years of age, was diagnosed with bone pain and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: actinomycosis, blood immunoglobulin m increased, bone debridement, bone disorder, bone pain, facial pain, fibrosis, impaired healing, neurolysis, . ZOMETA dosage: unknown. During the same period patient was treated with AREDIA. Patient recovered.

Clarithromycin Side Effects Report #5526227-3
Physician from JAPAN reported CLARITHROMYCIN problem on Nov 20, 2007. Male patient, 78 years of age, was diagnosed with pharyngitis, nail tinea, neuropathy peripheral, gastritis, anal fistula, insomnia and was treated with CLARITHROMYCIN. After drug was administered, patient experienced the following problems/side effects: blood immunoglobulin e increased, blood immunoglobulin g increased, blood immunoglobulin m increased, blood lactate dehydrogenase increased, c-reactive protein increased, eosinophil count increased, hyperhidrosis, lymphocyte morphology abnormal, . CLARITHROMYCIN dosage: 400 MG/D. During the same period patient was treated with HOCHUUEKKITOU, CONFATANIN, LAMISIL, MECOBALAMIN, MARZULENE S, NERIPROCT, DEPAS. Patient was hospitalized. Patient recovered.

Ortho Side Effects Report #5746618-5
ORTHO EVRA problem was reported by a Consumer or non-health professional from UNITED STATES on May 19, 2008. Female patient, weighting 135.5 lb, was diagnosed with acne cystic, contraception and was treated with ORTHO EVRA. After drug was administered, patient experienced the following problems/side effects: abdominal pain, blood calcium decreased, blood immunoglobulin m increased, blood potassium decreased, cough, cytomegalovirus antibody positive, deep vein thrombosis, dyspnoea, excoriation, . ORTHO EVRA dosage: unknown. During the same period patient was treated with ORTHO EVRA, IBUPROFEN. Patient was hospitalized. Patient recovered.

Gleevec Side Effects Report #5323453-3
Physician from AUSTRALIA reported GLEEVEC problem on May 04, 2007. Female patient, 69 years of age, was diagnosed with metastases to liver and was treated with GLEEVEC. After drug was administered, patient experienced the following problems/side effects: anaemia, biopsy bone marrow abnormal, blood immunoglobulin m increased, diarrhoea, protein total increased, reflux oesophagitis, rouleaux formation, tumour necrosis, waldenstrom's macroglobulinaemia, . GLEEVEC dosage: 400 MG, QD. During the same period patient was treated with VITAMINS. Patient was hospitalized. Patient recovered.

Fenofibrate Side Effects Report #5295523-X
FENOFIBRATE problem was reported by a Physician from JAPAN on Mar 21, 2007. Female patient, 66 years of age, was diagnosed with biliary cirrhosis and was treated with FENOFIBRATE. After drug was administered, patient experienced the following problems/side effects: anorexia, antibody test positive, blood immunoglobulin m increased, eosinophil count increased, hepatocellular damage, lymphocyte stimulation test positive, pyrexia, . FENOFIBRATE dosage: 150MG, QD. During the same period patient was treated with URSODEOXYCHOLIC ACID. Patient was hospitalized. Patient recovered.