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BLOOD IRON INCREASED side effect

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Aleve Side Effects Report #5659045-6
Consumer or non-health professional from UNITED STATES reported ALEVE problem on Sept 27, 2007. Male patient, 41 years of age, weighting 160.9 lb, was diagnosed with pain, vitamin supplementation and was treated with ALEVE. After drug was administered, patient experienced the following problems/side effects: blood iron increased, . ALEVE dosage: unknown. During the same period patient was treated with ONE A DAY MEN, ONE A DAY PRODUCT. Patient recovered.

Infergen Side Effects Report #5642320-9
INFERGEN problem was reported by a Physician from UNITED STATES on Feb 07, 2008. Female patient, weighting 172.0 lb, was diagnosed with hepatitis c and was treated with INFERGEN. After drug was administered, patient experienced the following problems/side effects: blood iron increased, haemolytic anaemia, headache, pain, stress, transfusion reaction, weight decreased, . INFERGEN dosage: unknown. During the same period patient was treated with RIBAVIRIN, HYDROCHLOROTHIAZIDE, AVAPRO, PROCRIT, SILYMARIN. Patient recovered.

Rebif Side Effects Report #5647973-7
Health Professional from UNITED STATES reported REBIF problem on Feb 15, 2008. Female patient, 63 years of age, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: blood iron increased, gastrointestinal disorder, hepatic enzyme increased, serum ferritin increased, . REBIF dosage: unknown. During the same period patient was treated with IRON SUPPLEMENTS. Patient recovered.

Infergen Side Effects Report #5649891-7
INFERGEN problem was reported by a Physician from UNITED STATES on Feb 07, 2008. Female patient, weighting 172.0 lb, was diagnosed with hepatitis c and was treated with INFERGEN. After drug was administered, patient experienced the following problems/side effects: blood iron increased, fatigue, haemolytic anaemia, headache, pain, pyrexia, stress, transfusion reaction, weight decreased, . INFERGEN dosage: unknown. During the same period patient was treated with RIBAVIRIN, HYDROCHLOROTHIAZIDE, AVAPRO, PROCRIT, SILYMARIN. Patient recovered.


Femara Side Effects Report #5533209-4
Consumer or non-health professional from AUSTRALIA reported FEMARA problem on Nov 30, 2007. Female patient was diagnosed with breast cancer and was treated with FEMARA. After drug was administered, patient experienced the following problems/side effects: blood iron increased, cataract, cataract operation, dry eye, vision blurred, . FEMARA dosage: 2.5 MG, QD. During the same period patient was treated with OMEGA, TEMAZEPAM, CIPRAMIL. Patient recovered.

Lamisil Side Effects Report #5508388-5
LAMISIL problem was reported by a Consumer or non-health professional from AUSTRALIA on Nov 01, 2007. Male patient, 57 years of age, was diagnosed with onychomycosis and was treated with LAMISIL. After drug was administered, patient experienced the following problems/side effects: blood iron increased, burning sensation, dermatitis exfoliative, diarrhoea, dysgeusia, dyspepsia, fat intolerance, feeling hot, hiatus hernia, . LAMISIL dosage: 250 MG, QD. During the same period patient was treated with AVAPRO, ACETAMINOPHEN W, IBUPROFEN. Patient recovered.

Exjade Side Effects Report #5528686-9
Consumer or non-health professional from NETHERLANDS reported EXJADE problem on Nov 22, 2007. Male patient, 61 years of age, was diagnosed with haemochromatosis and was treated with EXJADE. After drug was administered, patient experienced the following problems/side effects: blood iron increased, coordination abnormal, electromyogram abnormal, hypoaesthesia, joint stiffness, muscular weakness, oedema peripheral, paraesthesia, peripheral motor neuropathy, . EXJADE dosage: 20 MG/KG/D. During the same period patient was treated with BLOOD TRANSFUSION. Patient recovered.

Exjade Side Effects Report #5491870-7
EXJADE problem was reported by a Consumer or non-health professional from NETHERLANDS on Sept 24, 2007. Male patient, 61 years of age, was diagnosed with haemochromatosis and was treated with EXJADE. After drug was administered, patient experienced the following problems/side effects: blood iron increased, electromyogram abnormal, hypoaesthesia, joint stiffness, muscular weakness, oedema peripheral, paraesthesia, peripheral motor neuropathy, polyneuropathy, . EXJADE dosage: 20 MG/KG/D. During the same period patient was treated with BLOOD TRANSFUSION. Patient recovered.

Exjade Side Effects Report #5495581-3
Consumer or non-health professional from AUSTRALIA reported EXJADE problem on Oct 18, 2007. Male patient was diagnosed with myelodysplastic syndrome and was treated with EXJADE. After drug was administered, patient experienced the following problems/side effects: blood iron increased, leukaemia, treatment noncompliance, . EXJADE dosage: unknown. Patient recovered.


Micardis Side Effects Report #5454782-0
MICARDIS HCT problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 11, 2007. Male patient, 63 years of age, was diagnosed with hypertension and was treated with MICARDIS HCT. After drug was administered, patient experienced the following problems/side effects: blood iron increased, . MICARDIS HCT dosage: unknown. During the same period patient was treated with ASPIRIN. Patient recovered.

Micardis Side Effects Report #5460818-3
Consumer or non-health professional from UNITED STATES reported MICARDIS HCT problem on Sept 11, 2007. Male patient, 63 years of age, was diagnosed with hypertension and was treated with MICARDIS HCT. After drug was administered, patient experienced the following problems/side effects: blood iron increased, . MICARDIS HCT dosage: unknown. During the same period patient was treated with ASPIRIN. Patient recovered.

Tamoxifen Side Effects Report #5423909-9
TAMOXIFEN CITRATE problem was reported by a Health Professional from AUSTRALIA on Aug 08, 2007. Female patient, 70 years of age, was diagnosed with breast cancer female and was treated with TAMOXIFEN CITRATE. After drug was administered, patient experienced the following problems/side effects: blood iron increased, cataract, dry eye, haemolysis, vision blurred, . TAMOXIFEN CITRATE dosage: unknown. During the same period patient was treated with FERMARA, FISH OIL. Patient recovered.

Propecia Side Effects Report #5755586-1
Physician from JAPAN reported PROPECIA problem on May 26, 2008. Male patient, 42 years of age, weighting 138.9 lb, was diagnosed with androgenetic alopecia and was treated with PROPECIA. After drug was administered, patient experienced the following problems/side effects: blood iron increased, . PROPECIA dosage: unknown. Patient recovered.

Combivir Side Effects Report #5761183-4
COMBIVIR problem was reported by a Consumer or non-health professional from FRANCE on May 29, 2008. Male patient, 43 years of age, was diagnosed with hiv infection and was treated with COMBIVIR. After drug was administered, patient experienced the following problems/side effects: blood iron increased, pancytopenia, progressive multifocal leukoencephalopathy, renal failure acute, . COMBIVIR dosage: unknown. During the same period patient was treated with CRIXIVAN, VIREAD, KALETRA, BIPROFENID. Patient was hospitalized. Patient recovered.


Aleve Side Effects Report #5762857-1
Consumer or non-health professional from UNITED STATES reported ALEVE problem on May 07, 2008. Male patient, 41 years of age, weighting 160.9 lb, was diagnosed with pain, vitamin supplementation and was treated with ALEVE. After drug was administered, patient experienced the following problems/side effects: blood iron increased, . ALEVE dosage: unknown. During the same period patient was treated with ONE A DAY MEN, ONE A DAY PRODUCT. Patient recovered.

Zetia Side Effects Report #5764743-X
ZETIA problem was reported by a Physician from UNITED STATES on June 04, 2008. Female patient, 63 years of age, weighting 167.6 lb, was diagnosed with multiple sclerosis and was treated with ZETIA. After drug was administered, patient experienced the following problems/side effects: blood iron increased, gastrointestinal disorder, hepatic steatosis, serum ferritin increased, . ZETIA dosage: unknown. During the same period patient was treated with REBIF, LIPITOR, ASPIRIN, BLOPRESS PLUS. Patient recovered.

Propecia Side Effects Report #5749664-0
Physician from JAPAN reported PROPECIA problem on May 16, 2008. Male patient, 42 years of age, weighting 138.9 lb, was diagnosed with androgenetic alopecia and was treated with PROPECIA. After drug was administered, patient experienced the following problems/side effects: blood iron increased, . PROPECIA dosage: unknown. Patient recovered.

Rebif Side Effects Report #5756814-9
REBIF problem was reported by a Physician from UNITED STATES on May 14, 2008. Female patient, 63 years of age, weighting 167.0 lb, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: blood iron increased, gastrointestinal disorder, hepatic steatosis, serum ferritin increased, . REBIF dosage: unknown. During the same period patient was treated with LIPITOR, ZETIA, ASPIRIN, ATACAND. Patient recovered.

Ribavirin Side Effects Report #5712113-2
Physician from UNITED STATES reported RIBAVIRIN problem on Feb 07, 2008. Female patient, weighting 172.0 lb, was diagnosed with hepatitis c and was treated with RIBAVIRIN. After drug was administered, patient experienced the following problems/side effects: blood iron increased, fatigue, haemolytic anaemia, headache, pain, pyrexia, stress, transfusion reaction, weight decreased, . RIBAVIRIN dosage: (600 MG [200 MG QAM AND 400 MG QPM] ORAL), (200 MG TID ORAL). During the same period patient was treated with INFERGEN, HYDROCHLOROTHIAZIDE, AVAPRO, PROCRIT, SILYMARIN. Patient recovered.


Seroquel Side Effects Report #5719471-3
SEROQUEL problem was reported by a Health Professional from UNITED STATES on Apr 21, 2008. Female patient, 48 years of age, was treated with SEROQUEL. After drug was administered, patient experienced the following problems/side effects: blood iron increased, . SEROQUEL dosage: unknown. Patient recovered.

Exjade Side Effects Report #5381905-4
Consumer or non-health professional from UNITED STATES reported EXJADE problem on Mar 13, 2007. Female patient, 40 years of age, weighting 106.9 lb, was treated with EXJADE. After drug was administered, patient experienced the following problems/side effects: blood iron increased, blood urea increased, candidiasis, haematocrit decreased, haemoglobin decreased, oral pain, paraesthesia, red blood cell count decreased, serum ferritin increased, . EXJADE dosage: 1000 MG, QD, ORAL : 500 MG, QD, ORAL : 500 MG, QD, ORAL : 500 MG, QD, ORAL. During the same period patient was treated with VITAMINS, DETROL. Patient recovered.

Lanvis Side Effects Report #5311540-5
LANVIS problem was reported by a Consumer or non-health professional from FRANCE on Apr 17, 2007. Male patient, child 7 years of age, was treated with LANVIS. After drug was administered, patient experienced the following problems/side effects: blood iron increased, blood lactate dehydrogenase increased, histiocytosis haematophagic, inflammation, pancytopenia, peritoneal effusion, petechiae, pyrexia, retinal haemorrhage, . LANVIS dosage: 60MG PER DAY. During the same period patient was treated with ARACYTINE, ENDOXAN, BACTRIM. Patient was hospitalized. Patient recovered.

Nexium Side Effects Report #5312069-0
Consumer or non-health professional from UNITED STATES reported NEXIUM problem on June 28, 2006. Female patient, 74 years of age, weighting 110.0 lb, was diagnosed with gastritis and was treated with NEXIUM. After drug was administered, patient experienced the following problems/side effects: blood iron increased, . NEXIUM dosage: unknown. During the same period patient was treated with VYTORIN, TOPROL, HYDROCHLOROTHIAZIDE, MONOPRIL, PLAVIX, ASPIRIN, ALLOPURINOL. Patient recovered.

Exjade Side Effects Report #5335944-X
EXJADE problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 16, 2007. Male patient, 74 years of age, was diagnosed with myelodysplastic syndrome and was treated with EXJADE. After drug was administered, patient experienced the following problems/side effects: blood iron increased, . EXJADE dosage: 1250 MG QD ORAL. During the same period patient was treated with REVLIMID. Patient recovered.

Isotretinoin Side Effects Report #5259473-7
Consumer or non-health professional from UNITED STATES reported ISOTRETINOIN problem on Sept 06, 2006. Male patient, 22 years of age, was treated with ISOTRETINOIN. After drug was administered, patient experienced the following problems/side effects: blood iron increased, gamma-glutamyltransferase increased, haemochromatosis, liver function test abnormal, . ISOTRETINOIN dosage: 40 MG, QD. Patient recovered.

Exjade Side Effects Report #5335921-9
EXJADE problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 18, 2006. Female patient was diagnosed with anaemia and was treated with EXJADE. After drug was administered, patient experienced the following problems/side effects: blood iron increased, rash, . EXJADE dosage: 1000MG, UNK, ORAL. During the same period patient was treated with ARANESP. Patient recovered.

Chantix Side Effects Report #5555840-2
Physician from UNITED STATES reported CHANTIX problem on Dec 01, 2007. Female patient, weighting 164.0 lb, was diagnosed with hypersensitivity and was treated with CHANTIX. After drug was administered, patient experienced the following problems/side effects: autoimmune hepatitis, blood iron increased, jaundice, malaise, . CHANTIX dosage: unknown. During the same period patient was treated with NASONEX, ALAVERT. Patient recovered.

Zyban Side Effects Report #5510701-X
ZYBAN problem was reported by a Consumer or non-health professional from CANADA on Nov 02, 2007. Male patient, 41 years of age, weighting 251.5 lb, was diagnosed with anxiety and was treated with ZYBAN. After drug was administered, patient experienced the following problems/side effects: anxiety, blood iron increased, constipation, dry mouth, gout, heart rate increased, influenza, stomach discomfort, suicidal ideation, . ZYBAN dosage: 150MG TWICE PER DAY. During the same period patient was treated with VALIUM. Patient recovered.

Vistabex Side Effects Report #5515247-0
Consumer or non-health professional from ITALY reported VISTABEX problem on Nov 08, 2007. Female patient was treated with VISTABEX. After drug was administered, patient experienced the following problems/side effects: asthenia, blood iron increased, bone pain, bronchial disorder, dermatomyositis, dysphagia, dyspnoea, erythema multiforme, face oedema, . VISTABEX dosage: unknown. Patient was hospitalized. Patient recovered.

Vistabex Side Effects Report #5515277-9
VISTABEX problem was reported by a Consumer or non-health professional from ITALY on Nov 08, 2007. Female patient was treated with VISTABEX. After drug was administered, patient experienced the following problems/side effects: asthenia, blood iron increased, bone pain, bronchial disorder, dermatomyositis, dysphagia, dyspnoea, erythema multiforme, face oedema, . VISTABEX dosage: unknown. Patient was hospitalized. Patient recovered.

Zyban Side Effects Report #5478336-5
Consumer or non-health professional from CANADA reported ZYBAN problem on Oct 03, 2007. Male patient, 41 years of age, weighting 251.5 lb, was treated with ZYBAN. After drug was administered, patient experienced the following problems/side effects: anxiety, blood iron increased, constipation, dry mouth, gout, heart rate increased, influenza, suicidal ideation, thirst, . ZYBAN dosage: 150MG TWICE PER DAY. During the same period patient was treated with VALIUM. Patient recovered.

Chantix Side Effects Report #5453155-4
CHANTIX problem was reported by a Physician from UNITED STATES on Sept 04, 2007. Female patient, weighting 164.0 lb, was diagnosed with hypersensitivity and was treated with CHANTIX. After drug was administered, patient experienced the following problems/side effects: autoimmune hepatitis, blood iron increased, jaundice, malaise, . CHANTIX dosage: unknown. During the same period patient was treated with NASONEX, ALAVERT. Patient recovered.

Zyban Side Effects Report #5459478-7
Consumer or non-health professional from CANADA reported ZYBAN problem on Sept 18, 2007. Male patient, 41 years of age, weighting 251.5 lb, was treated with ZYBAN. After drug was administered, patient experienced the following problems/side effects: anxiety, blood iron increased, dry mouth, gout, heart rate increased, influenza, suicidal ideation, thirst, vomiting, . ZYBAN dosage: 150MG TWICE PER DAY. During the same period patient was treated with VALIUM. Patient recovered.

Zyban Side Effects Report #5408685-8
ZYBAN problem was reported by a Consumer or non-health professional from CANADA on July 24, 2007. Male patient, weighting 251.5 lb, was treated with ZYBAN. After drug was administered, patient experienced the following problems/side effects: anxiety, blood iron increased, dry mouth, gout, heart rate increased, influenza, suicidal ideation, thirst, vomiting, . ZYBAN dosage: 150MG TWICE PER DAY. During the same period patient was treated with VALIUM. Patient recovered.

Zyban Side Effects Report #5426170-4
Consumer or non-health professional from CANADA reported ZYBAN problem on Aug 23, 2007. Male patient, weighting 251.5 lb, was treated with ZYBAN. After drug was administered, patient experienced the following problems/side effects: anxiety, blood iron increased, dry mouth, gout, heart rate increased, influenza, suicidal ideation, thirst, vomiting, . ZYBAN dosage: 150MG TWICE PER DAY. During the same period patient was treated with VALIUM. Patient recovered.

Omniscan Side Effects Report #5741908-4
OMNISCAN problem was reported by a Physician from UNITED STATES on May 05, 2008. Male patient, 68 years of age, was treated with OMNISCAN. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, blood iron increased, dialysis, hypotension, inflammation, iron binding capacity total decreased, nephrogenic systemic fibrosis, renal injury, serum ferritin increased, . OMNISCAN dosage: 40 ML, SINGLE DOSE, I.V.. Patient died.

Propulsid Side Effects Report #5695844-2
Consumer or non-health professional from SWEDEN reported PROPULSID problem on Mar 27, 2008. Female patient, 43 years of age, was diagnosed with constipation and was treated with PROPULSID. After drug was administered, patient experienced the following problems/side effects: alopecia, blood iron increased, ocular hyperaemia, osteoporosis, pollakiuria, visual disturbance, white blood cell count increased, . PROPULSID dosage: unknown. During the same period patient was treated with PROGESTERON, PROPAVAN. Patient recovered.

Lamictal Side Effects Report #5697677-X
LAMICTAL problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 28, 2008. Female patient, 53 years of age, was diagnosed with anxiety and was treated with LAMICTAL. After drug was administered, patient experienced the following problems/side effects: autoimmune hepatitis, blood iron increased, enzyme abnormality, malaise, nausea, rash, . LAMICTAL dosage: 75MG PER DAY. During the same period patient was treated with KLONOPIN. Patient recovered.

Tegretol Side Effects Report #5304138-6
Physician from GERMANY reported TEGRETOL problem on Apr 10, 2007. Male patient, 35 years of age, weighting 145.5 lb, was diagnosed with bipolar disorder and was treated with TEGRETOL. After drug was administered, patient experienced the following problems/side effects: blood cholesterol increased, blood iron increased, gamma-glutamyltransferase increased, haematocrit decreased, mean cell haemoglobin concentration increased, phlebotomy, red blood cell count decreased, serum ferritin increased, white blood cell count increased, . TEGRETOL dosage: 600 MG/DAY. Patient recovered.

Librax Side Effects Report #5273408-2
LIBRAX problem was reported by a Consumer or non-health professional from on Mar 05, 2007. Male patient, 65 years of age, was diagnosed with diverticulum and was treated with LIBRAX. After drug was administered, patient experienced the following problems/side effects: angina pectoris, blood iron increased, chondrocalcinosis, dysuria, electrocardiogram abnormal, flatulence, hepatocellular damage, infrequent bowel movements, muscle spasms, . LIBRAX dosage: unknown. During the same period patient was treated with PLAVIX, KARGEDIC, BISOPROLOL, MOVICOL, TRANSILANE. Patient recovered.

Zyban Side Effects Report #5623101-9
Consumer or non-health professional from CANADA reported ZYBAN problem on Feb 05, 2008. Male patient, 41 years of age, weighting 251.5 lb, was treated with ZYBAN. After drug was administered, patient experienced the following problems/side effects: anorexia, anxiety, blood iron increased, bursitis, constipation, decreased appetite, dry mouth, gout, . ZYBAN dosage: 150MG TWICE PER DAY. During the same period patient was treated with VALIUM. Patient recovered.

Zyban Side Effects Report #5586989-6
ZYBAN problem was reported by a Consumer or non-health professional from CANADA on Jan 04, 2008. Male patient, 41 years of age, weighting 251.5 lb, was treated with ZYBAN. After drug was administered, patient experienced the following problems/side effects: anorexia, anxiety, blood iron increased, bursitis, constipation, dry mouth, gout, heart rate increased, . ZYBAN dosage: 150MG TWICE PER DAY. During the same period patient was treated with VALIUM. Patient recovered.

Zyban Side Effects Report #5541749-7
Consumer or non-health professional from CANADA reported ZYBAN problem on Dec 04, 2007. Male patient, 41 years of age, weighting 251.5 lb, was treated with ZYBAN. After drug was administered, patient experienced the following problems/side effects: anorexia, anxiety, blood iron increased, bursitis, constipation, dry mouth, gout, heart rate increased, . ZYBAN dosage: 150MG TWICE PER DAY. During the same period patient was treated with VALIUM. Patient recovered.

Clozaril Side Effects Report #5566589-4
CLOZARIL problem was reported by a Health Professional from AUSTRALIA on Dec 11, 2007. Male patient, 30 years of age, was treated with CLOZARIL. After drug was administered, patient experienced the following problems/side effects: agitation, alanine aminotransferase increased, blood iron increased, convulsion, delusion, emotional distress, gamma-glutamyltransferase increased, haemangioma, haemochromatosis, . CLOZARIL dosage: unknown. Patient was hospitalized. Patient recovered.

Rebif Side Effects Report #5507146-5
Health Professional from UNITED STATES reported REBIF problem on Oct 21, 2007. Female patient, 63 years of age, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood iron increased, gamma-glutamyltransferase increased, gastrointestinal disorder, serum ferritin increased, . REBIF dosage: unknown. During the same period patient was treated with IRON SUPPLEMENTS. Patient recovered.

Clozaril Side Effects Report #5522256-4
CLOZARIL problem was reported by a Physician from AUSTRALIA on Nov 13, 2007. Male patient, 30 years of age, was treated with CLOZARIL. After drug was administered, patient experienced the following problems/side effects: agitation, alanine aminotransferase increased, blood iron increased, convulsion, delusion, emotional distress, gamma-glutamyltransferase increased, haemangioma, haemochromatosis, . CLOZARIL dosage: unknown. Patient was hospitalized. Patient recovered.

Claritin Side Effects Report #5772877-9
Physician from UNITED STATES reported CLARITIN problem on Mar 05, 2008. Female patient, weighting 117.0 lb, was diagnosed with ear disorder, sinusitis and was treated with CLARITIN. After drug was administered, patient experienced the following problems/side effects: anger, anxiety, blood iron increased, blood pressure increased, chest pain, dehydration, diarrhoea, dizziness, dry mouth, . CLARITIN dosage: unknown. During the same period patient was treated with GABAPENTIN, TRAMADOL, VALTREX, XANAX. Patient recovered.

Claritin Side Effects Report #5694097-9
CLARITIN problem was reported by a Physician from UNITED STATES on Mar 05, 2008. Female patient, weighting 117.0 lb, was diagnosed with ear disorder, sinusitis and was treated with CLARITIN. After drug was administered, patient experienced the following problems/side effects: anger, anxiety, blood iron increased, blood pressure fluctuation, blood pressure increased, chest pain, dehydration, diarrhoea, dizziness, . CLARITIN dosage: unknown. During the same period patient was treated with GABAPENTIN, TRAMADOL, VALTREX, XANAX. Patient recovered.

Zyban Side Effects Report #5694640-X
Consumer or non-health professional from CANADA reported ZYBAN problem on Apr 02, 2008. Male patient, 41 years of age, weighting 251.5 lb, was treated with ZYBAN. After drug was administered, patient experienced the following problems/side effects: anorexia, anxiety, blood iron increased, bursitis, constipation, decreased appetite, dry mouth, gout, . ZYBAN dosage: 150MG TWICE PER DAY. During the same period patient was treated with VALIUM. Patient recovered.

Mesulid Side Effects Report #5699639-5
MESULID problem was reported by a Physician from GREECE on Mar 31, 2008. Female patient, 61 years of age, was treated with MESULID. After drug was administered, patient experienced the following problems/side effects: aspartate aminotransferase increased, blood alkaline phosphatase increased, blood iron increased, hepatic enzyme increased, serum ferritin increased, . MESULID dosage: unknown. During the same period patient was treated with ASPIRIN, EXFORGE. Patient was hospitalized. Patient recovered.