Menu

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

BLOOD FOLATE DECREASED side effect

What is BLOOD FOLATE DECREASED ?

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

Type your question here

 letters left

Lyrica Side Effects Report #5603181-7
Physician from GREECE reported LYRICA problem on Jan 15, 2008. Male patient, 37 years of age, weighting 220.5 lb, was diagnosed with neuralgia and was treated with LYRICA. After drug was administered, patient experienced the following problems/side effects: blood folate decreased, blood glucose increased, gingival bleeding, periodontal disease, . LYRICA dosage: unknown. During the same period patient was treated with VENLAFAXINE, LEXOTANIL, LONARID. Patient recovered.

Lyrica Side Effects Report #5578367-0
LYRICA problem was reported by a Physician from GREECE on Dec 19, 2007. Male patient, 37 years of age, weighting 220.5 lb, was diagnosed with neuralgia and was treated with LYRICA. After drug was administered, patient experienced the following problems/side effects: blood folate decreased, blood glucose increased, gingival bleeding, periodontal disease, . LYRICA dosage: unknown. During the same period patient was treated with VENLAFAXINE, LEXOTANIL, LONARID. Patient recovered.

Remicade Side Effects Report #5376836-X
Physician from JAPAN reported REMICADE problem on June 21, 2007. Female patient, weighting 110.2 lb, was diagnosed with rheumatoid arthritis, osteoporosis, antibiotic prophylaxis, analgesia and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: blood folate decreased, pancytopenia, . REMICADE dosage: unknown. During the same period patient was treated with RHEUMATREX, ALFAROL, ISCOTIN, INFREE, ULGUT, ASPARA. Patient was hospitalized. Patient recovered.

Remicade Side Effects Report #5376836-X
REMICADE problem was reported by a Physician from JAPAN on June 21, 2007. Female patient, weighting 110.2 lb, was diagnosed with rheumatoid arthritis, osteoporosis, antibiotic prophylaxis, analgesia and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: blood folate decreased, pancytopenia, . REMICADE dosage: unknown. During the same period patient was treated with RHEUMATREX, ALFAROL, ISCOTIN, INFREE, ULGUT, ASPARA. Patient was hospitalized. Patient recovered.


Lyrica Side Effects Report #5703143-5
Physician from GREECE reported LYRICA problem on Mar 31, 2008. Male patient, 37 years of age, weighting 220.5 lb, was diagnosed with neuralgia and was treated with LYRICA. After drug was administered, patient experienced the following problems/side effects: blood folate decreased, blood glucose increased, gingival bleeding, periodontal disease, . LYRICA dosage: unknown. During the same period patient was treated with VENLAFAXINE, LEXOTANIL, LONARID. Patient recovered.

Betaseron Side Effects Report #5342502-X
BETASERON problem was reported by a Consumer or non-health professional from UNITED STATES on May 17, 2007. Female patient, 54 years of age, was diagnosed with relapsing-remitting multiple sclerosis and was treated with BETASERON. After drug was administered, patient experienced the following problems/side effects: blood folate decreased, cyclothymic disorder, delusion, depression, dissociative disorder, fatigue, multiple sclerosis, oedema peripheral, personality disorder, . BETASERON dosage: unknown. During the same period patient was treated with FOLIC ACID, VITAMIN B, REMERON, BEXTRA, KEPPRA, NEXIUM, POTASSIUM CHLORIDE. Patient was hospitalized. Patient recovered.

Isradipine Side Effects Report #5663428-8
Health Professional from CHILE reported ISRADIPINE problem on Mar 02, 2008. Male patient, 78 years of age, was diagnosed with hypertension and was treated with ISRADIPINE. After drug was administered, patient experienced the following problems/side effects: anaemia, blood folate decreased, blood immunoglobulin e increased, echography abnormal, hyperthyroidism, interstitial lung disease, pulmonary fibrosis, weight decreased, . ISRADIPINE dosage: 5 MG;PO. During the same period patient was treated with AMIODARONE, HYTACAND, FLECAINIDE ACETATE, NEO MERCAZOLE, CARBIMAZOLE, PROPYLTHIOURACIL, ERTHROCYTE CONCENTRATE. Patient recovered.

Diovan Side Effects Report #5635004-4
DIOVAN problem was reported by a Consumer or non-health professional from BRAZIL on Feb 15, 2008. Female patient, 45 years of age, weighting 134.5 lb, was diagnosed with hypertension and was treated with DIOVAN. After drug was administered, patient experienced the following problems/side effects: anaemia, blood folate decreased, chest discomfort, fatigue, feeling abnormal, haemoglobin decreased, joint swelling, menstruation delayed, . DIOVAN dosage: 80 MG, QD. During the same period patient was treated with EXFORGE. Patient recovered.

Diovan Side Effects Report #5599582-6
Consumer or non-health professional from BRAZIL reported DIOVAN problem on Jan 15, 2008. Female patient, 45 years of age, weighting 134.5 lb, was diagnosed with hypertension and was treated with DIOVAN. After drug was administered, patient experienced the following problems/side effects: anaemia, blood folate decreased, chest discomfort, fatigue, feeling abnormal, haemoglobin decreased, joint swelling, menstruation delayed, . DIOVAN dosage: 80 MG, QD. During the same period patient was treated with EXFORGE. Patient recovered.


Viread Side Effects Report #5492341-4
VIREAD problem was reported by a Health Professional from FRANCE on Oct 10, 2007. Male patient, 50 years of age, was treated with VIREAD. After drug was administered, patient experienced the following problems/side effects: back pain, blood folate decreased, extrapyramidal disorder, fanconi syndrome acquired, muscular weakness, nerve conduction studies abnormal, osteomalacia, pain in extremity, . VIREAD dosage: unknown. During the same period patient was treated with EPIVIR, VIRACEPT, DEPAKINE. Patient was hospitalized. Patient recovered.

Viread Side Effects Report #5377808-1
Health Professional from FRANCE reported VIREAD problem on June 21, 2007. Male patient, 50 years of age, was treated with VIREAD. After drug was administered, patient experienced the following problems/side effects: back pain, blood folate decreased, extrapyramidal disorder, fanconi syndrome acquired, muscular weakness, nerve conduction studies abnormal, osteomalacia, pain in extremity, . VIREAD dosage: unknown. During the same period patient was treated with EPIVIR, VIRACEPT. Patient was hospitalized. Patient recovered.

Viread Side Effects Report #5377808-1
VIREAD problem was reported by a Health Professional from FRANCE on June 21, 2007. Male patient, 50 years of age, was treated with VIREAD. After drug was administered, patient experienced the following problems/side effects: back pain, blood folate decreased, extrapyramidal disorder, fanconi syndrome acquired, muscular weakness, nerve conduction studies abnormal, osteomalacia, pain in extremity, . VIREAD dosage: unknown. During the same period patient was treated with EPIVIR, VIRACEPT. Patient was hospitalized. Patient recovered.

Citalopram Side Effects Report #5724380-X
Consumer or non-health professional from FRANCE reported CITALOPRAM HYDROBROMIDE problem on Apr 14, 2008. Male patient, 35 years of age, was treated with CITALOPRAM HYDROBROMIDE. After drug was administered, patient experienced the following problems/side effects: aspiration, blood folate decreased, lung disorder, pancytopenia, septic shock, spinal myelogram abnormal, . CITALOPRAM HYDROBROMIDE dosage: 20 MG QD;PO. During the same period patient was treated with LAMICTAL, MOZINAN, HALDOL, TEGRETOL, IMOVANE, URBANYL, SEGLOR. Patient was hospitalized. Patient recovered.

Aldactone Side Effects Report #5364748-7
ALDACTONE problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 24, 2007. Female patient, 59 years of age, weighting 120.0 lb, was diagnosed with fluid retention and was treated with ALDACTONE. After drug was administered, patient experienced the following problems/side effects: anaemia, blood folate decreased, gastric ulcer, haematochezia, . ALDACTONE dosage: 25 MG (25 MG, QD: EVERY DAY). Patient recovered.


Byetta Side Effects Report #5234977-1
Consumer or non-health professional from UNITED STATES reported BYETTA problem on Sept 15, 2006. Male patient was diagnosed with diabetes mellitus and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: blood amino acid level decreased, blood folate decreased, blood glucose increased, blood magnesium decreased, vitamin b12 decreased, . BYETTA dosage: unknown. During the same period patient was treated with GLIPIZIDE, METFORMIN. Patient recovered.

Valsartan Side Effects Report #5273622-6
VALSARTAN AND HYDROCHLOROTHIAZIDE problem was reported by a Consumer or non-health professional from FRANCE on Mar 12, 2007. Male patient, 75 years of age, was diagnosed with hypertension and was treated with VALSARTAN AND HYDROCHLOROTHIAZIDE. After drug was administered, patient experienced the following problems/side effects: anaemia macrocytic, blood folate decreased, blood immunoglobulin e increased, c-reactive protein increased, fatigue, full blood count decreased, gastroenteritis, haemoglobin decreased, leukaemia, . VALSARTAN AND HYDROCHLOROTHIAZIDE dosage: unknown. Patient recovered.

Zelitrex Side Effects Report #5446352-5
Physician from FRANCE reported ZELITREX problem on Aug 28, 2007. Female patient, 87 years of age, weighting 176.4 lb, was diagnosed with herpes zoster, dermatosis and was treated with ZELITREX. After drug was administered, patient experienced the following problems/side effects: anaemia macrocytic, blood folate decreased, blood thyroid stimulating hormone increased, dermatosis, eczema, eczema weeping, eosinophil count increased, fungal infection, . ZELITREX dosage: unknown. During the same period patient was treated with CIFLOX, FLAGYL, ARICEPT, LEVOTHYROX, ZOLOFT, RISPERDAL, ATARAX, TELFAST. Patient was hospitalized. Patient recovered.

Zelitrex Side Effects Report #5337260-9
ZELITREX problem was reported by a Physician from FRANCE on May 23, 2007. Female patient, 87 years of age, weighting 176.4 lb, was diagnosed with herpes zoster, dermatosis and was treated with ZELITREX. After drug was administered, patient experienced the following problems/side effects: anaemia macrocytic, blood folate decreased, blood thyroid stimulating hormone increased, dermatosis, eczema, eczema weeping, eosinophil count increased, fungal infection, . ZELITREX dosage: unknown. During the same period patient was treated with CIFLOX, FLAGYL, ARICEPT, LEVOTHYROXINE, ZOLOFT, RISPERDAL, ATARAX, TELFAST. Patient was hospitalized. Patient recovered.