Combivir and haemoglobin decreased 
Combivir and haemoglobin decreased Patient Reports February 11, 2012
Combivir Side Effects Report #4582799-7
Combivir side effect was reported by a Physician from on Feb 01, 2005. Male patient, 54 years of age, weighting 178.6 lb, was diagnosed with systemic antiviral treatment, ill-defined disorder and was treated with Combivir. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, haemoglobin decreased, renal failure. Combivir dosage: unknown. During the same period patient was treated with EFAVIRENZ. Patient died.
Combivir Side Effects Report #4603956-7
Combivir side effect was reported by a Physician from on Mar 02, 2005. Male patient, 38 years of age, weighting 127.9 lb, was diagnosed with systemic antiviral treatment, ill-defined disorder and was treated with Combivir. After drug was administered, patient experienced the following side effects: haemoglobin decreased, haemoglobinaemia, oedema peripheral, pain in extremity, palpitations, platelet count increased, white blood cell count decreased. Combivir dosage: 300MG TWICE PER DAY. During the same period patient was treated with EFAVIRENZ, DAPSONE. Patient recovered.
Combivir Side Effects Report #4605983-2
Combivir side effect was reported by a Physician from on Mar 02, 2005. Male patient, 38 years of age, weighting 127.9 lb, was diagnosed with systemic antiviral treatment, ill-defined disorder and was treated with Combivir. After drug was administered, patient experienced the following side effects: haemoglobin decreased, haemoglobinaemia, oedema peripheral, pain in extremity, palpitations, platelet count increased, white blood cell count decreased. Combivir dosage: 300MG TWICE PER DAY. During the same period patient was treated with EFAVIRENZ, DAPSONE. Patient recovered.
Combivir Side Effects Report #4663506-6
Combivir side effect was reported by a Health Professional from on May 11, 2005. Male patient, 48 years of age, was diagnosed with ill-defined disorder and was treated with Combivir. After drug was administered, patient experienced the following side effects: anaemia, haemoglobin decreased, thrombocytopenia. Combivir dosage: unknown. During the same period patient was treated with KALETRA, BACTRIM, RETROVIR. Patient recovered.
Combivir Side Effects Report #5664505-8
Combivir side effect was reported by a Physician from UGANDA on Mar 10, 2008. Female patient, child 9 years of age, was diagnosed with hiv infection
and was treated with Combivir. After drug was administered, patient experienced the following side effects: abdominal pain , bronchopneumonia, cough, haemoglobin decreased, neuropathy peripheral, neutropenia, pain in extremity, pyrexia. Combivir dosage: unknown. During the same period patient was treated with EFAVIRENZ, ABACAVIR, COTRIMOXAZOLE, VALPROATE. Patient was hospitalized. Patient recovered.Combivir Side Effects Report #4895399-6
Combivir side effect was reported by a Consumer or non-health professional from UNITED STATES on Feb 18, 2005. Male patient, 57 years of age, was diagnosed with hiv infection
and was treated with Combivir. After drug was administered, patient experienced the following side effects: haematocrit decreased, haemoglobin decreased. Combivir dosage: unknown. During the same period patient was treated with GLIPIZIDE, VIRAMUNE. Patient recovered.Combivir Side Effects Report #5392412-7
Combivir side effect was reported by a Consumer or non-health professional from FRANCE on July 12, 2007. Male patient, 47 years of age, was diagnosed with hiv infection
, hepatitis c and was treated with Combivir. After drug was administered, patient experienced the following side effects: anaemia, asthenia, blood lactate dehydrogenase increased, haemoglobin decreased. Combivir dosage: unknown. During the same period patient was treated with COPEGUS, SUSTIVA, PEGASYS. Patient was hospitalized. Patient recovered.Combivir Side Effects Report #5396657-1
Combivir side effect was reported by a Consumer or non-health professional from FRANCE on July 23, 2007. Male patient, 47 years of age, was diagnosed with hiv infection
, hepatitis c and was treated with Combivir. After drug was administered, patient experienced the following side effects: anaemia, asthenia, blood lactate dehydrogenase increased, haemoglobin decreased. Combivir dosage: unknown. During the same period patient was treated with COPEGUS, SUSTIVA, PEGASYS. Patient was hospitalized. Patient recovered.Combivir Side Effects Report #5875141-2
Combivir side effect was reported by a Physician from GERMANY on Sept 03, 2008. Male patient, 45 years of age, weighting 158.7 lb, was diagnosed with hiv infection
and was treated with Combivir. After drug was administered, patient experienced the following side effects: anaemia macrocytic, bone marrow failure, haemoglobin decreased, hyperchromic anaemia, myelodysplastic syndrome. Combivir dosage: 450MG TWICE PER DAY. During the same period patient was treated with SUSTIVA. Patient was hospitalized. Patient recovered.Combivir Side Effects Report #4556049-1
Combivir side effect was reported by a Physician from on Jan 05, 2005. Male patient, 34 years of age, was diagnosed with hiv infection
and was treated with Combivir. After drug was administered, patient experienced the following side effects: asthenia, chest pain , dizziness , haemoglobin decreased, neutropenic sepsis. Combivir dosage: unknown. During the same period patient was treated with TENOFOVIR, ISONIAZID, PYRAZINAMIDE, RIFAMPICIN, ETHAMBUTOL. Patient was hospitalized. Patient recovered.Combivir Side Effects Report #5530653-6
Combivir side effect was reported by a Consumer or non-health professional from UNITED KINGDOM on Nov 20, 2007. Male patient, 25 years of age, was diagnosed with hiv infection
and was treated with Combivir. After drug was administered, patient experienced the following side effects: agitation, alanine aminotransferase increased, biopsy liver abnormal, blood alkaline phosphatase increased, blood bilirubin increased, confusional state, cough, haemoglobin decreased, pain in extremity. Combivir dosage: unknown. During the same period patient was treated with EFAVIRENZ, TENOFOVIR DISOPROXIL FUMARATE, LAMIVUDINE, NEVIRAPINE, COTRIM, LOPERAMIDE HYDROCHLORIDE. Patient was hospitalized. Patient died.Combivir Side Effects Report #5841823-1
Combivir side effect was reported by a Consumer or non-health professional from UNITED KINGDOM on Aug 07, 2008. Male patient, 25 years of age, was diagnosed with hiv infection
and was treated with Combivir. After drug was administered, patient experienced the following side effects: agitation, alanine aminotransferase increased, biopsy liver abnormal, blood alkaline phosphatase increased, blood bilirubin increased, confusional state, cough, haemoglobin decreased, hepatotoxicity. Combivir dosage: unknown. During the same period patient was treated with EFAVIRENZ, TENOFOVIR, LAMIVUDINE, VIRAMUNE, SEPTRIN, LOPERAMIDE HYDROCHLORIDE. Patient was hospitalized. Patient died on 06/22/2003.Combivir Side Effects Report #6000098-3
Combivir side effect was reported by a Physician from RUSSIAN FEDERATION on Dec 09, 2008. Female patient, 25 years of age, weighting 121.3 lb, was diagnosed with hiv infection
and was treated with Combivir. After drug was administered, patient experienced the following side effects: anaemia, cardiac murmur, dizziness , haemoglobin decreased, headache , malaise, pallor, red blood cell count decreased. Combivir dosage: unknown. During the same period patient was treated with STOCRIN, ABACAVIR, LAMIVUDINE. Patient recovered.Combivir Side Effects Report #5370792-6
Combivir side effect was reported by a Consumer or non-health professional from FRANCE on June 15, 2007. Female patient, weighting 4.85 lb, was diagnosed with hiv infection
and was treated with Combivir. After drug was administered, patient experienced the following side effects: abdominal discomfort, abdominal distension, haemoglobin decreased, haemolysis, hyperkalaemia, hyperlactacidaemia, premature baby, renal failure. Combivir dosage: unknown. During the same period patient was treated with KALETRA, INVIRASE, SPASFON, TARDYFERON B, VITAMIN K, KAYEXALATE. Patient was hospitalized. Patient recovered.Combivir Side Effects Report #5374834-3
Combivir side effect was reported by a Health Professional from UNITED KINGDOM on June 21, 2007. Female patient was diagnosed with hiv infection
and was treated with Combivir. After drug was administered, patient experienced the following side effects: ascites, cardiomyopathy , cytomegalovirus infection , developmental delay, foetal-maternal haemorrhage, haemoglobin decreased, hydrops foetalis, pericardial effusion. Combivir dosage: unknown. During the same period patient was treated with VIRAMUNE. Patient recovered.Combivir Side Effects Report #5423668-X
Combivir side effect was reported by a Health Professional from UNITED KINGDOM on Aug 15, 2007. Male patient was diagnosed with hiv infection
and was treated with Combivir. After drug was administered, patient experienced the following side effects: ascites, cardiomyopathy , cytomegalovirus infection , developmental delay, foetal-maternal haemorrhage, haemoglobin decreased, hydrops foetalis, pericardial effusion. Combivir dosage: unknown. During the same period patient was treated with VIRAMUNE. Patient recovered.Combivir Side Effects Report #5612348-3
Combivir side effect was reported by a Consumer or non-health professional from UNITED STATES on Feb 01, 2008. Female patient, weighting 115.7 lb, was diagnosed with hiv infection
and was treated with Combivir. After drug was administered, patient experienced the following side effects: asthenia, fatigue, haematocrit decreased, haemoglobin decreased. Combivir dosage: unknown. During the same period patient was treated with LEXIVA. Patient recovered.Combivir Side Effects Report #4950481-X
Combivir side effect was reported by a Physician from SWITZERLAND on Feb 27, 2003. Female patient, weighting 119.0 lb, was diagnosed with hiv infection
and was treated with Combivir. After drug was administered, patient experienced the following side effects: anaemia macrocytic, aplasia pure red cell, blood erythropoietin increased, dyspnoea exertional, haemoglobin decreased, hypoplastic anaemia, leukopenia, oedema peripheral, pallor. Combivir dosage: 150MG TWICE PER DAY. During the same period patient was treated with KALETRA, DIPIPERON, CITALOPRAM HYDROBROMIDE, TORSEMIDE, METHADONE, BACTRIM, TENOFOVIR. Patient was hospitalized. Patient recovered.Combivir Side Effects Report #4954086-6
Combivir side effect was reported by a Physician from SWITZERLAND on Feb 27, 2003. Female patient, weighting 119.0 lb, was diagnosed with hiv infection
and was treated with Combivir. After drug was administered, patient experienced the following side effects: anaemia macrocytic, aplasia pure red cell, blood erythropoietin increased, dyspnoea exertional, haemoglobin decreased, hypoplastic anaemia, leukopenia, oedema peripheral, pallor. Combivir dosage: 150MG TWICE PER DAY. During the same period patient was treated with KALETRA, DIPIPERON, CITALOPRAM HYDROBROMIDE, TORSEMIDE, METHADONE, BACTRIM, TENOFOVIR. Patient was hospitalized. Patient recovered.Combivir Side Effects Report #4632776-2
Combivir side effect was reported by a Health Professional from on Apr 08, 2005. Female patient, 46 years of age, weighting 102.0 lb, was diagnosed with biliary cirrhosis and was treated with Combivir. After drug was administered, patient experienced the following side effects: abdominal distension, ascites, haemoglobin decreased, oedema peripheral. Combivir dosage: LAMIVUDINE 150 MG; ZIDOVUDINE 300 MG QD PO. During the same period patient was treated with OXYBUTININ, RESTORIL, VIT D, HYDROXYZINE, URSO, VIT E, LORAZEPAM, NASONEX. Patient was hospitalized. Patient recovered.
Combivir Side Effects Report #5836863-2
Combivir side effect was reported by a Physician from BOTSWANA on Aug 04, 2008. Female patient, 36 years of age, was diagnosed with antiviral prophylaxis and was treated with Combivir. After drug was administered, patient experienced the following side effects: foetal heart rate abnormal, haemoglobin decreased, umbilical cord around neck. Combivir dosage: unknown. During the same period patient was treated with KALETRA. Patient died.
Combivir Side Effects Report #4760393-2
Combivir side effect was reported by a Physician from JAPAN on July 15, 2005. Female patient, 59 years of age, weighting 85.98 lb, was diagnosed with acquired immunodeficiency syndrome, hiv infection
and was treated with Combivir. After drug was administered, patient experienced the following side effects: anaemia, cardiac failure, haemoglobin decreased. Combivir dosage: unknown. During the same period patient was treated with STOCRIN, MEBRON, ZITHROMAC, EPIVIR, CLARITHROMYCIN, PREDONINE, TRYPTANOL, OMEPRAZOLE. Patient was hospitalized. Patient recovered.Combivir Side Effects Report #4817016-3
Combivir side effect was reported by a Physician from JAPAN on July 15, 2005. Female patient, 59 years of age, weighting 85.98 lb, was diagnosed with acquired immunodeficiency syndrome, hiv infection
, temporal arteritis, depression and was treated with Combivir. After drug was administered, patient experienced the following side effects: anaemia, cardiac failure, condition aggravated, haemoglobin decreased. Combivir dosage: unknown. During the same period patient was treated with STOCRIN, MEBRON, ZITHROMAC, EPIVIR, CLARITHROMYCIN, PREDONINE, TRYPTANOL, OMEPRAL. Patient was hospitalized. Patient recovered.Combivir Side Effects Report #5168950-9
Combivir side effect was reported by a Physician from UNITED STATES on Dec 05, 2006. Female patient, 58 years of age, was treated with Combivir. After drug was administered, patient experienced the following side effects: anaemia, aplasia pure red cell, blood product transfusion dependent, haemoglobin decreased, haemolysis, haemolytic anaemia, polycythaemia, reticulocyte count decreased. Combivir dosage: unknown. During the same period patient was treated with PROCRIT, CRIXIVAN, AMITRIPTYLINE, SERETIDE DISKUS MITE, ANTICHOLINERGICS. Patient was hospitalized. Patient recovered.
Combivir Side Effects Report #4686271-5
Combivir side effect was reported by a Consumer or non-health professional from on June 02, 2005. Male patient, 49 years of age, was diagnosed with hiv infection
and was treated with Combivir. After drug was administered, patient experienced the following side effects: aplastic anaemia, blood bilirubin increased, blood lactate dehydrogenase increased, bone marrow depression, haemoglobin decreased, pancytopenia, thrombocytopenia. Combivir dosage: unknown. During the same period patient was treated with SAQUINAVIR MESILATE, ESOMEPRAZOLE MAGNESIUM, MIRTAZAPINE, PREDNISOLONE, RITONAVIR, CLINDAMYCIN HYDROCHLORIDE, URSODEOXYCHOLIC ACID, COLECALCIFEROL. Patient was hospitalized. Patient recovered.