Menu

• Ask a Health Expert about BLOOD URIC ACID DECREASED
• Post Your Side Effect related to BLOOD URIC ACID DECREASED
• BLOOD URIC ACID DECREASED and FDA Warnings
• BLOOD URIC ACID DECREASED in Patients Wiki
• Report BLOOD URIC ACID DECREASED in Drug Side Effect Survey

BLOOD URIC ACID DECREASED side effect

What is BLOOD URIC ACID DECREASED ?

A Health Expert wants to answer your question. Please provide details below.

Type your question here

 letters left

Gleevec Side Effects Report #5610812-4
Health Professional from FRANCE reported GLEEVEC problem on Jan 22, 2008. Female patient, 50 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: blood uric acid decreased, fanconi syndrome, glycosuria, hypomagnesaemia, hypophosphataemia, myalgia, renal failure, renal tubular disorder, . GLEEVEC dosage: 400 MG/D. Patient recovered.

Novantrone Side Effects Report #5536416-X
NOVANTRONE problem was reported by a Consumer or non-health professional from JAPAN on Nov 26, 2007. Male patient, 58 years of age, was diagnosed with acute myeloid leukaemia recurrent and was treated with NOVANTRONE. After drug was administered, patient experienced the following problems/side effects: anaemia, blood lactate dehydrogenase increased, blood uric acid decreased, c-reactive protein increased, condition aggravated, febrile neutropenia, gastrointestinal haemorrhage, haematemesis, haematuria, . NOVANTRONE dosage: unknown. During the same period patient was treated with MYLOTARG, ITRACONAZOLE, MAXIPIME. Patient was hospitalized. Patient died on 05/01/2007.

Tacrolimus Side Effects Report #5387651-5
Physician from JAPAN reported TACROLIMUS problem on July 02, 2007. Female patient, 85 years of age, weighting 83.56 lb, was diagnosed with rheumatoid arthritis and was treated with TACROLIMUS. After drug was administered, patient experienced the following problems/side effects: beta 2 microglobulin urine increased, blood albumin decreased, blood uric acid decreased, fall, femur fracture, haematocrit decreased, myocardial infarction, . TACROLIMUS dosage: 1.5 MG, UID/QD, ORAL. During the same period patient was treated with METHYLPREDNISOLONE, MOBIC, ISCOTIN, SELBEX. Patient was hospitalized. Patient recovered.

Tacrolimus Side Effects Report #5387651-5
TACROLIMUS problem was reported by a Physician from JAPAN on July 02, 2007. Female patient, 85 years of age, weighting 83.56 lb, was diagnosed with rheumatoid arthritis and was treated with TACROLIMUS. After drug was administered, patient experienced the following problems/side effects: beta 2 microglobulin urine increased, blood albumin decreased, blood uric acid decreased, fall, femur fracture, haematocrit decreased, myocardial infarction, . TACROLIMUS dosage: 1.5 MG, UID/QD, ORAL. During the same period patient was treated with METHYLPREDNISOLONE, MOBIC, ISCOTIN, SELBEX. Patient was hospitalized. Patient recovered.


Imuran Side Effects Report #5705794-0
Health Professional from UNITED STATES reported IMURAN problem on Dec 28, 2006. Male patient, 18 years of age, weighting 163.1 lb, was diagnosed with crohn's disease and was treated with IMURAN. After drug was administered, patient experienced the following problems/side effects: anorexia, blood lactate dehydrogenase increased, blood uric acid decreased, bone pain, convulsion, diarrhoea, headache, hypotension, joint swelling, . IMURAN dosage: 75 MG; PO; 100 MG; PO; 150 MG; PO. During the same period patient was treated with REMICADE, PREDNISONE, ENTOCORT EC, CALCIUM. Patient was hospitalized. Patient died on 09/22/2002.