Menu

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

BLOOD LACTIC ACID INCREASED side effect

What is BLOOD LACTIC ACID INCREASED ?

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

Type your question here

 letters left

Propofol Side Effects Report #5669511-5
Health Professional from FRANCE reported PROPOFOL problem on Mar 06, 2008. Male patient, 66 years of age, weighting 145.5 lb, was diagnosed with induction of anaesthesia, maintenance of anaesthesia, essential hypertension and was treated with PROPOFOL. After drug was administered, patient experienced the following problems/side effects: blood lactic acid increased, . PROPOFOL dosage: unknown. During the same period patient was treated with LIDOCAINE, NEBIVOLOL, VALSARTAN AND HYDROCHLOROTHIAZIDE. Patient recovered.

Viramune Side Effects Report #5673579-X
VIRAMUNE problem was reported by a Physician from FRANCE on Nov 23, 2006. Female patient, weighting 6.61 lb, was diagnosed with human immunodeficiency virus transmission, hiv infection and was treated with VIRAMUNE. After drug was administered, patient experienced the following problems/side effects: blood lactic acid increased, hypertriglyceridaemia, neutropenia, . VIRAMUNE dosage: unknown. During the same period patient was treated with VIDEX, INVIRASE, NORVIR, SUSTIVA, VIRACEPT, RETROVIR. Patient was hospitalized. Patient recovered.

Combivir Side Effects Report #5678996-X
Consumer or non-health professional from UNITED STATES reported COMBIVIR problem on Mar 18, 2008. Male patient, 31 years of age, was diagnosed with antiviral prophylaxis and was treated with COMBIVIR. After drug was administered, patient experienced the following problems/side effects: blood lactic acid increased, hepatic enzyme increased, muscle spasms, . COMBIVIR dosage: unknown. During the same period patient was treated with PROTEIN, MILK THISTLE, NELFINAVIR. Patient recovered.

Baraclude Side Effects Report #5682488-1
BARACLUDE problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 14, 2008. Male patient, 34 years of age, was diagnosed with hepatitis b and was treated with BARACLUDE. After drug was administered, patient experienced the following problems/side effects: blood lactic acid increased, . BARACLUDE dosage: unknown. Patient recovered.


Cefepime Side Effects Report #5537460-9
Health Professional from BRAZIL reported CEFEPIME problem on Dec 05, 2007. Female patient, 22 years of age, was diagnosed with sepsis, pyelonephritis acute and was treated with CEFEPIME. After drug was administered, patient experienced the following problems/side effects: blood lactic acid increased, hypotension, non-cardiogenic pulmonary oedema, pneumonia, . CEFEPIME dosage: unknown. Patient recovered.

Metformin Side Effects Report #5566274-9
METFORMIN problem was reported by a Pharmacist from UNITED STATES on Dec 13, 2007. Male patient, 69 years of age, was diagnosed with diabetes mellitus and was treated with METFORMIN. After drug was administered, patient experienced the following problems/side effects: blood lactic acid increased, . METFORMIN dosage: 500MG BID PO. Patient was hospitalized. Patient recovered.

Clolar Side Effects Report #5570303-6
Consumer or non-health professional from UNITED STATES reported CLOLAR problem on Dec 19, 2007. Male patient, weighting 151.7 lb, was treated with CLOLAR. After drug was administered, patient experienced the following problems/side effects: blood lactic acid increased, caecitis, colitis, enterobacter infection, enterococcal infection, fungal infection, hypotension, pseudomonas infection, refusal of treatment by relative, . CLOLAR dosage: 73 MG. During the same period patient was treated with CYTARABINE. Patient was hospitalized. Patient recovered.

Zoloft Side Effects Report #5495284-5
ZOLOFT problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 12, 2007. Male patient, 18 years of age, weighting 155.0 lb, was diagnosed with anxiety and was treated with ZOLOFT. After drug was administered, patient experienced the following problems/side effects: blood lactic acid increased, . ZOLOFT dosage: unknown. Patient recovered.

Aprotinin Side Effects Report #5462988-X
Health Professional from UNITED STATES reported APROTININ problem on Sept 11, 2007. Female patient, 78 years of age, was diagnosed with aortic valve replacement, blood product transfusion, platelet transfusion and was treated with APROTININ. After drug was administered, patient experienced the following problems/side effects: blood lactic acid increased, coagulopathy, haemorrhage, hypotension, intracardiac thrombus, oliguria, pulmonary oedema, ventricular failure, . APROTININ dosage: unknown. During the same period patient was treated with PROTAMINE SULPHATE, FRESH FROZEN PLASMA, PLATELETS, RED BLOOD CELLS, LEVOTHYROXINE, TRIAMTERENE. Patient died.


Ibuprofen Side Effects Report #5463831-5
IBUPROFEN problem was reported by a Pharmacist from UNITED STATES on Sept 04, 2007. Male patient, 28 years of age, was diagnosed with intentional overdose and was treated with IBUPROFEN. After drug was administered, patient experienced the following problems/side effects: blood lactic acid increased, coagulopathy, gastrointestinal necrosis, haemodialysis, haemodynamic instability, hepatic failure, hepatic necrosis, . IBUPROFEN dosage: unknown. During the same period patient was treated with ACETAMINOPHEN. Patient was hospitalized. Patient recovered.

Sertraline Side Effects Report #5413297-6
Consumer or non-health professional from INDIA reported SERTRALINE problem on July 13, 2007. Female patient, 45 years of age, was diagnosed with depression and was treated with SERTRALINE. After drug was administered, patient experienced the following problems/side effects: blood lactic acid increased, crying, feelings of worthlessness, parkinsonism, . SERTRALINE dosage: 50 MG, QD; 100 MG, QD. During the same period patient was treated with ALPRAZOLAM, CLONAZEPAM, PROMETHAZINE HYDROCHLORIDE, TRIHEXYPHENIDYL, DOTHIEPIN HYDROCHLORIDE. Patient was hospitalized. Patient recovered.

Aotal Side Effects Report #5415592-3
AOTAL problem was reported by a Pharmacist from FRANCE on Aug 03, 2007. Female patient, 50 years of age, was treated with AOTAL. After drug was administered, patient experienced the following problems/side effects: blood lactic acid increased, contusion, decreased activity, fall, haemoglobin decreased, melaena, somnolence, subdural haematoma, . AOTAL dosage: unknown. During the same period patient was treated with BISOPROLOL FUMARATE, MEPRONIZINE, ASPIRIN, AMLODIPINE BESYLATE, PRAVASTATIN. Patient was hospitalized. Patient recovered.

Vandral Side Effects Report #5417880-3
Health Professional from SPAIN reported VANDRAL RETARD problem on Aug 09, 2007. Female patient, weighting 198.4 lb, was diagnosed with fibromyalgia and was treated with VANDRAL RETARD. After drug was administered, patient experienced the following problems/side effects: blood lactic acid increased, discomfort, hepatitis, nausea, pruritus, swelling face, vomiting, . VANDRAL RETARD dosage: unknown. During the same period patient was treated with GELOCATIL, TRAMADOL, PAROXETINE. Patient recovered.

Januvia Side Effects Report #5468724-5
JANUVIA problem was reported by a Physician from UNITED STATES on June 19, 2007. Male patient was diagnosed with type 2 diabetes mellitus and was treated with JANUVIA. After drug was administered, patient experienced the following problems/side effects: blood lactic acid increased, . JANUVIA dosage: 100 MG, DAILY; PO. Patient recovered.


Effexor Side Effects Report #5376711-0
Health Professional from FRANCE reported EFFEXOR problem on June 22, 2007. Female patient, 36 years of age, was treated with EFFEXOR. After drug was administered, patient experienced the following problems/side effects: blood lactic acid increased, blood pressure decreased, coma, haemodynamic instability, intentional overdose, miosis, oxygen saturation decreased, . EFFEXOR dosage: OVERDOSE AMOUNT: 750 MG. During the same period patient was treated with THERALENE, ETHANOL, DEPAMIDE. Patient was hospitalized. Patient recovered.

Effexor Side Effects Report #5376711-0
EFFEXOR problem was reported by a Health Professional from FRANCE on June 22, 2007. Female patient, 36 years of age, was treated with EFFEXOR. After drug was administered, patient experienced the following problems/side effects: blood lactic acid increased, blood pressure decreased, coma, haemodynamic instability, intentional overdose, miosis, oxygen saturation decreased, . EFFEXOR dosage: OVERDOSE AMOUNT: 750 MG. During the same period patient was treated with THERALENE, ETHANOL, DEPAMIDE. Patient was hospitalized. Patient recovered.

Mercaptopurine Side Effects Report #5758158-8
Consumer or non-health professional from UNITED STATES reported MERCAPTOPURINE problem on June 02, 2008. Female patient, weighting 74.08 lb, was treated with MERCAPTOPURINE. After drug was administered, patient experienced the following problems/side effects: blood lactic acid increased, candiduria, coagulopathy, haemorrhage, hepatic function abnormal, metabolic acidosis, multi-organ failure, nervous system disorder, neutropenia, . MERCAPTOPURINE dosage: 1275 MG. During the same period patient was treated with METHOTREXATE, VINCRISTINE SULPHATE, DEXAMETHASONE. Patient was hospitalized. Patient recovered.

Prinivil Side Effects Report #5769264-6
PRINIVIL problem was reported by a Health Professional from UNITED STATES on June 03, 2008. Female patient, 78 years of age, weighting 128.0 lb, was diagnosed with osteoporosis and was treated with PRINIVIL. After drug was administered, patient experienced the following problems/side effects: blood lactic acid increased, colitis ischaemic, escherichia urinary tract infection, hypotension, hypovolaemia, metabolic acidosis, myocardial infarction, renal failure acute, syncope, . PRINIVIL dosage: unknown. During the same period patient was treated with LASOFOXIFENE UNK, ALENDRONATE, ASCORBIC ACID, ASPIRIN, CALCIUM, CYANOCOBALAMIN, FERROUS SULPHATE, ISOPHANE INSULIN. Patient was hospitalized. Patient recovered.

Cisplatin Side Effects Report #5774917-X
Consumer or non-health professional from UNITED STATES reported CISPLATIN problem on June 16, 2008. Female patient, weighting 188.4 lb, was treated with CISPLATIN. After drug was administered, patient experienced the following problems/side effects: blood lactic acid increased, coagulopathy, colitis ischaemic, confusional state, hyperglycaemia, hypernatraemia, mental status changes, neutropenia, . CISPLATIN dosage: 93 MG. During the same period patient was treated with DOXORUBICIN HYDROCHLORIDE, TAXOL, NEULASTA. Patient was hospitalized. Patient recovered.


Metformin Side Effects Report #5787489-0
METFORMIN problem was reported by a Pharmacist from UNITED STATES on June 23, 2008. Male patient, 55 years of age, was diagnosed with diabetes mellitus and was treated with METFORMIN. After drug was administered, patient experienced the following problems/side effects: blood lactic acid increased, hypotension, muscle spasms, renal failure acute, . METFORMIN dosage: 500 MG TID PO. Patient recovered.

Mercaptopurine Side Effects Report #5753699-1
Consumer or non-health professional from UNITED STATES reported MERCAPTOPURINE problem on May 27, 2008. Female patient, weighting 74.08 lb, was treated with MERCAPTOPURINE. After drug was administered, patient experienced the following problems/side effects: blood lactic acid increased, cerebral haemorrhage, coagulopathy, fungal infection, hepatic function abnormal, metabolic acidosis, multi-organ failure, neutropenia, pyrexia, . MERCAPTOPURINE dosage: 1275 MG. During the same period patient was treated with METHOTREXATE, VINCRISTINE SULPHATE, DEXAMETHASONE. Patient was hospitalized. Patient recovered.

Glucophage Side Effects Report #5713898-1
GLUCOPHAGE problem was reported by a Pharmacist from UNITED STATES on Apr 22, 2008. Female patient, weighting 309.0 lb, was diagnosed with type 2 diabetes mellitus and was treated with GLUCOPHAGE. After drug was administered, patient experienced the following problems/side effects: blood lactic acid increased, . GLUCOPHAGE dosage: 1000MG BID PO. During the same period patient was treated with DIOVAN, MAXZIDE, LASIX, ZOCOR, PREVACID, REMERON, NORVASC, NITROGLYCERIN. Patient was hospitalized. Patient recovered.

Acetaminophen Side Effects Report #5369659-9
Health Professional from TURKEY reported ACETAMINOPHEN problem on June 08, 2007. Female patient was treated with ACETAMINOPHEN. After drug was administered, patient experienced the following problems/side effects: blood lactic acid increased, confusional state, diarrhoea, hepatomegaly, hepatotoxicity, liver injury, metabolic acidosis, . ACETAMINOPHEN dosage: 15 MG/KG, QID. Patient was hospitalized. Patient recovered.

Zyvox Side Effects Report #5377155-8
ZYVOX problem was reported by a Pharmacist from UNITED STATES on June 29, 2007. Male patient, weighting 264.6 lb, was diagnosed with catheter sepsis and was treated with ZYVOX. After drug was administered, patient experienced the following problems/side effects: blood lactic acid increased, chills, hypotension, mouth ulceration, nausea, pharyngolaryngeal pain, pyrexia, sinus headache, . ZYVOX dosage: 600 MG TWICE DAILY PO. Patient was hospitalized. Patient recovered.

Minocycline Side Effects Report #5318721-5
Health Professional from CANADA reported MINOCYCLINE problem on Apr 24, 2007. Male patient, 39 years of age, was diagnosed with acne and was treated with MINOCYCLINE. After drug was administered, patient experienced the following problems/side effects: blood lactic acid increased, hypercholesterolaemia, hypertriglyceridaemia, . MINOCYCLINE dosage: (50 MG BID). During the same period patient was treated with TETRACYCLINE, DIDANOSINE, STAVUDINE, NEVIRAPINE, LOPINAVIR, TENOFOVIR, ALUMINUM HYDROXIDE GEL. Patient recovered.

Vandral Side Effects Report #5330750-4
VANDRAL RETARD problem was reported by a Health Professional from SPAIN on May 17, 2007. Female patient, weighting 198.4 lb, was diagnosed with fibromyalgia and was treated with VANDRAL RETARD. After drug was administered, patient experienced the following problems/side effects: blood lactic acid increased, discomfort, hepatitis, nausea, pruritus, swelling face, vomiting, . VANDRAL RETARD dosage: unknown. During the same period patient was treated with GELOCATIL, TRAMADOL, PAROXETINE. Patient recovered.

Vandral Side Effects Report #5302332-1
Health Professional from SPAIN reported VANDRAL RETARD problem on Apr 13, 2007. Female patient, weighting 198.4 lb, was diagnosed with fibromyalgia and was treated with VANDRAL RETARD. After drug was administered, patient experienced the following problems/side effects: blood lactic acid increased, discomfort, hepatitis, nausea, pruritus, swelling face, vomiting, . VANDRAL RETARD dosage: unknown. During the same period patient was treated with GELOCATIL, PAROXETINE. Patient recovered.

Vandral Side Effects Report #5308207-6
VANDRAL RETARD problem was reported by a Health Professional from SPAIN on Apr 18, 2007. Female patient, weighting 198.4 lb, was diagnosed with fibromyalgia and was treated with VANDRAL RETARD. After drug was administered, patient experienced the following problems/side effects: blood lactic acid increased, discomfort, hepatitis, nausea, pruritus, swelling face, vomiting, . VANDRAL RETARD dosage: unknown. During the same period patient was treated with GELOCATIL, TRAMADOL, PAROXETINE. Patient recovered.

Albuterol Side Effects Report #5316281-6
Consumer or non-health professional from UNITED STATES reported ALBUTEROL SULATE problem on Apr 24, 2007. Male patient, 16 years of age, was treated with ALBUTEROL SULATE. After drug was administered, patient experienced the following problems/side effects: blood lactic acid increased, blood ph decreased, coma, dyspnoea, oxygen saturation decreased, po2 decreased, tachycardia, treatment noncompliance, wheezing, . ALBUTEROL SULATE dosage: unknown. Patient recovered.

High Side Effects Report #5266009-3
HIGH FIBER DIET problem was reported by a Physician from COSTA RICA on Mar 02, 2007. Male patient, child 11 years of age, weighting 92.59 lb, was diagnosed with conduct disorder, constipation and was treated with HIGH FIBER DIET. After drug was administered, patient experienced the following problems/side effects: blood lactic acid increased, brain oedema, computerised tomogram abnormal, constipation, depressed level of consciousness, facial palsy, hemiplegia, increased appetite, intracranial pressure increased, . HIGH FIBER DIET dosage: unknown. During the same period patient was treated with IMIPRAMINE, VALPROIC ACID, ZELMAC, PSICOSOMA. Patient was hospitalized and became disabled. Patient recovered.

Epivir Side Effects Report #5275781-8
Consumer or non-health professional from FRANCE reported EPIVIR problem on Mar 22, 2007. Female patient, 52 years of age, weighting 94.80 lb, was treated with EPIVIR. After drug was administered, patient experienced the following problems/side effects: blood lactic acid increased, blood urea increased, grand mal convulsion, hyperglycaemia, hyponatraemia, myoclonus, somnolence, . EPIVIR dosage: 300MG PER DAY. During the same period patient was treated with NORVIR, TELZIR, ZIAGEN, LASIX, OMEPRAZOLE, CALCIDIA, PRIMPERAN, LANTUS. Patient was hospitalized. Patient recovered.

Capecitabine Side Effects Report #5657230-0
CAPECITABINE problem was reported by a Physician from UNITED STATES on Mar 07, 2008. Female patient, weighting 187.0 lb, was diagnosed with breast cancer and was treated with CAPECITABINE. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased, blood lactic acid increased, blood pressure increased, body temperature decreased, cardiac arrest, diarrhoea, dysarthria, dyspnoea, heart rate increased, . CAPECITABINE dosage: 1650 MG BID ORALLY. Patient died on 03/03/2008.

Warfarin Side Effects Report #5638009-2
Pharmacist from UNITED STATES reported WARFARIN problem on Feb 22, 2008. Male patient, 89 years of age, weighting 172.0 lb, was diagnosed with pulmonary embolism and was treated with WARFARIN. After drug was administered, patient experienced the following problems/side effects: acidosis, blood lactic acid increased, colon cancer metastatic, gastrointestinal haemorrhage, haemoglobin decreased, international normalised ratio increased, metastases to liver, sepsis, . WARFARIN dosage: unknown. Patient was hospitalized. Patient recovered.

Prograf Side Effects Report #5551214-9
PROGRAF problem was reported by a Physician from JAPAN on Nov 26, 2007. Female patient, child 6 years of age, was diagnosed with liver transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: blood glucose increased, blood lactic acid increased, . PROGRAF dosage: unknown. During the same period patient was treated with STEROIDMULATION. Patient recovered.

Zidovudine Side Effects Report #5569740-5
Consumer or non-health professional from NETHERLANDS reported ZIDOVUDINE problem on Dec 04, 2007. Male patient was diagnosed with prophylaxis against hiv infection, hiv test positive, premature rupture of membranes and was treated with ZIDOVUDINE. After drug was administered, patient experienced the following problems/side effects: atrioventricular block complete, blood lactic acid increased, cardiac output decreased, congestive cardiomyopathy, no therapeutic response, premature baby, . ZIDOVUDINE dosage: 4 MG/KG / PER DAY. During the same period patient was treated with LAMIVUDINE, LOPINAVIR AND RITONAVIR. Patient recovered.

Clolar Side Effects Report #5578853-3
CLOLAR problem was reported by a Physician from UNITED STATES on Dec 18, 2007. Male patient, 24 years of age, weighting 151.7 lb, was diagnosed with acute leukaemia, acute lymphocytic leukaemia and was treated with CLOLAR. After drug was administered, patient experienced the following problems/side effects: aspiration joint abnormal, blood lactic acid increased, caecitis, culture positive, enterobacter infection, enterocolitis infectious, fungal infection, hypotension, joint swelling, . CLOLAR dosage: 40 MG/M2, QDX5, INTRAVENOUS. During the same period patient was treated with CYTARABINE. Patient was hospitalized. Patient died on 12/15/2007.

Ibuprofen Side Effects Report #5506682-5
Consumer or non-health professional from UNITED STATES reported IBUPROFEN problem on Oct 05, 2007. Male patient, 14 years of age, was treated with IBUPROFEN. After drug was administered, patient experienced the following problems/side effects: apnoea, blood lactic acid increased, circulatory collapse, gastric haemorrhage, hypotension, intentional overdose, metabolic acidosis, pulmonary haemorrhage, renal failure, . IBUPROFEN dosage: unknown. Patient was hospitalized. Patient recovered.

Ixempra Side Effects Report #5523545-X
IXEMPRA BRISTOL problem was reported by a Health Professional from UNITED STATES on Nov 19, 2007. Female patient, 48 years of age, weighting 155.0 lb, was treated with IXEMPRA BRISTOL. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, blood lactic acid increased, blood pressure decreased, dehydration, heart rate increased, hepatic enzyme increased, necrotising colitis, neutropenic colitis, . IXEMPRA BRISTOL dosage: unknown. Patient was hospitalized. Patient recovered.

Januvia Side Effects Report #5532914-3
Physician from UNITED STATES reported JANUVIA problem on Aug 09, 2007. Male patient, 55 years of age, weighting 212.0 lb, was diagnosed with type 2 diabetes mellitus and was treated with JANUVIA. After drug was administered, patient experienced the following problems/side effects: abdominal pain lower, blood lactic acid increased, nausea, vomiting, . JANUVIA dosage: 100 MG/DAILY/PO. Patient recovered.

Losartan Side Effects Report #5485172-2
LOSARTAN POTASSIUM problem was reported by a Health Professional from NORWAY on Oct 09, 2007. Female patient, 49 years of age, was diagnosed with hypertension, diabetes mellitus and was treated with LOSARTAN POTASSIUM. After drug was administered, patient experienced the following problems/side effects: accidental overdose, blood lactic acid increased, circulatory collapse, gastroenteritis, haemodialysis, hyperventilation, hypoglycaemia, . LOSARTAN POTASSIUM dosage: 50 MG, UNK. During the same period patient was treated with METFORMIN, GLIBENKLAMID, ESIDRIX. Patient recovered.

Tramadol Side Effects Report #5500115-0
Health Professional from FRANCE reported TRAMADOL problem on Oct 12, 2007. Male patient, 33 years of age, was treated with TRAMADOL. After drug was administered, patient experienced the following problems/side effects: blood bicarbonate decreased, blood lactic acid increased, bundle branch block right, cardiac arrest, cardiac failure, cerebral disorder, continuous haemodiafiltration, convulsion, depressed level of consciousness, . TRAMADOL dosage: unknown. During the same period patient was treated with HYDROXYZINE, GABAPENTIN, CLONAZEPAM. Patient recovered.

Ontak Side Effects Report #5448922-7
ONTAK problem was reported by a Health Professional from UNITED STATES on Aug 22, 2007. Female patient, 66 years of age, weighting 134.5 lb, was treated with ONTAK. After drug was administered, patient experienced the following problems/side effects: acute myocardial infarction, blood lactic acid increased, bradycardia, capillary leak syndrome, cardiac arrest, electromechanical dissociation, haemolysis, hypotension, lymphocyte percentage decreased, . ONTAK dosage: unknown. During the same period patient was treated with VINCRISTINE SULPHATE, DOXORUBIVIN, CYTOXAN, PREDNISONE, LIPITOR, LISINOPRIL, HYDROCHLOROTHIAZDE. Patient died on 08/06/2007.

High Side Effects Report #5409283-2
Physician from COSTA RICA reported HIGH FIBER DIET problem on Aug 02, 2007. Male patient, child 11 years of age, weighting 92.59 lb, was diagnosed with conduct disorder, constipation and was treated with HIGH FIBER DIET. After drug was administered, patient experienced the following problems/side effects: blood amino acid level increased, blood lactic acid increased, brain oedema, computerised tomogram abnormal, constipation, depressed level of consciousness, facial palsy, hemiplegia, increased appetite, . HIGH FIBER DIET dosage: unknown. During the same period patient was treated with IMIPRAMINE, VALPROIC ACID, ZELNORM, PSICOSOMA. Patient was hospitalized and became disabled. Patient recovered.

Kaletra Side Effects Report #5412748-0
KALETRA problem was reported by a Health Professional from FRANCE on Aug 07, 2007. Female patient, weighting 6.61 lb, was treated with KALETRA. After drug was administered, patient experienced the following problems/side effects: arrhythmia, blood lactic acid increased, encephalopathy, foetal distress syndrome, meconium in amniotic fluid, microcephaly, multi-organ failure, neonatal anoxia, unevaluable event, . KALETRA dosage: unknown. During the same period patient was treated with LAMIVUDINE. Patient was hospitalized. Patient recovered.

High Side Effects Report #5296271-2
Physician from COSTA RICA reported HIGH FIBER DIET problem on Apr 02, 2007. Male patient, child 11 years of age, weighting 92.59 lb, was diagnosed with conduct disorder, constipation and was treated with HIGH FIBER DIET. After drug was administered, patient experienced the following problems/side effects: blood amino acid level increased, blood lactic acid increased, brain oedema, computerised tomogram abnormal, constipation, depressed level of consciousness, facial palsy, hemiplegia, increased appetite, . HIGH FIBER DIET dosage: unknown. During the same period patient was treated with IMIPRAMINE, VALPROIC ACID, ZELNORM, PSICOSOMA. Patient was hospitalized and became disabled. Patient recovered.

Aotal Side Effects Report #5380524-3
AOTAL problem was reported by a Health Professional from FRANCE on June 22, 2007. Female patient, 50 years of age, was treated with AOTAL. After drug was administered, patient experienced the following problems/side effects: blood alcohol increased, blood lactic acid increased, cognitive disorder, fall, haemoglobin decreased, melaena, neuralgia, subdural haematoma, . AOTAL dosage: unknown. During the same period patient was treated with BISOPROLOL FUMARATE, MEPRONIZINE, KARDEGIC, AMLODIPINE BESYLATE, PRAVASTATIN. Patient was hospitalized. Patient recovered.

Aotal Side Effects Report #5393041-1
Health Professional from FRANCE reported AOTAL problem on July 06, 2007. Female patient, 50 years of age, was treated with AOTAL. After drug was administered, patient experienced the following problems/side effects: blood alcohol increased, blood lactic acid increased, fall, ischaemic stroke, melaena, subdural haematoma, . AOTAL dosage: unknown. During the same period patient was treated with BISOPROLOL FUMARATE, MEPRONIZINE, KARDEGIC, AMLODIPINE BESYLATE, PRAVASTATIN. Patient was hospitalized. Patient recovered.

Viread Side Effects Report #5398010-3
VIREAD problem was reported by a Consumer or non-health professional from FRANCE on July 16, 2007. Male patient, 52 years of age, was diagnosed with hiv infection and was treated with VIREAD. After drug was administered, patient experienced the following problems/side effects: anorexia, blood lactic acid increased, hepatic pain, hepatic steatosis, hepatomegaly, hypertriglyceridaemia, lactic acidosis, myalgia, neck pain, . VIREAD dosage: unknown. During the same period patient was treated with RETROVIR, NORVIR, PREZISTA. Patient was hospitalized. Patient recovered.

High Side Effects Report #5296271-2
Physician from COSTA RICA reported HIGH FIBER DIET problem on Apr 02, 2007. Male patient, child 11 years of age, weighting 92.59 lb, was diagnosed with conduct disorder, constipation and was treated with HIGH FIBER DIET. After drug was administered, patient experienced the following problems/side effects: blood amino acid level increased, blood lactic acid increased, brain oedema, computerised tomogram abnormal, constipation, depressed level of consciousness, facial palsy, hemiplegia, increased appetite, . HIGH FIBER DIET dosage: unknown. During the same period patient was treated with IMIPRAMINE, VALPROIC ACID, ZELNORM, PSICOSOMA. Patient was hospitalized and became disabled. Patient recovered.

Aotal Side Effects Report #5380524-3
AOTAL problem was reported by a Health Professional from FRANCE on June 22, 2007. Female patient, 50 years of age, was treated with AOTAL. After drug was administered, patient experienced the following problems/side effects: blood alcohol increased, blood lactic acid increased, cognitive disorder, fall, haemoglobin decreased, melaena, neuralgia, subdural haematoma, . AOTAL dosage: unknown. During the same period patient was treated with BISOPROLOL FUMARATE, MEPRONIZINE, KARDEGIC, AMLODIPINE BESYLATE, PRAVASTATIN. Patient was hospitalized. Patient recovered.

Aotal Side Effects Report #5393041-1
Health Professional from FRANCE reported AOTAL problem on July 06, 2007. Female patient, 50 years of age, was treated with AOTAL. After drug was administered, patient experienced the following problems/side effects: blood alcohol increased, blood lactic acid increased, fall, ischaemic stroke, melaena, subdural haematoma, . AOTAL dosage: unknown. During the same period patient was treated with BISOPROLOL FUMARATE, MEPRONIZINE, KARDEGIC, AMLODIPINE BESYLATE, PRAVASTATIN. Patient was hospitalized. Patient recovered.