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ANAEMIA MEGALOBLASTIC side effect

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Paludrine Side Effects Report #5659513-7
Health Professional from UNITED KINGDOM reported PALUDRINE problem on Feb 27, 2008. Male patient, 39 years of age, was diagnosed with malaria prophylaxis and was treated with PALUDRINE. After drug was administered, patient experienced the following problems/side effects: anaemia megaloblastic, epistaxis, gingival bleeding, lethargy, mucosal inflammation, pancytopenia, urticaria, . PALUDRINE dosage: 200 MG. During the same period patient was treated with AVLOCLORE. Patient was hospitalized. Patient recovered.

Depakene Side Effects Report #5611595-4
DEPAKENE problem was reported by a Physician from FRANCE on Jan 24, 2008. Male patient, 23 years of age, was diagnosed with epilepsy and was treated with DEPAKENE. After drug was administered, patient experienced the following problems/side effects: anaemia megaloblastic, . DEPAKENE dosage: unknown. During the same period patient was treated with TOPIRAMAX. Patient was hospitalized. Patient recovered.

Zyprexa Side Effects Report #5620178-1
Physician from GERMANY reported ZYPREXA problem on Jan 29, 2008. Female patient was treated with ZYPREXA. After drug was administered, patient experienced the following problems/side effects: anaemia megaloblastic, . ZYPREXA dosage: 5 MG, UNK. During the same period patient was treated with RAMIPRIL, BISOPROLOL. Patient recovered.

Effexor Side Effects Report #5623085-3
EFFEXOR problem was reported by a Health Professional from FRANCE on Feb 05, 2008. Female patient, weighting 152.1 lb, was diagnosed with depression and was treated with EFFEXOR. After drug was administered, patient experienced the following problems/side effects: anaemia megaloblastic, bone marrow failure, erythroblastosis, haptoglobin decreased, . EFFEXOR dosage: unknown. During the same period patient was treated with LEVOTHYROX, PIASCLEDINE, BROMAZEPAM, PARACETAMOL. Patient recovered.


Metformin Side Effects Report #5533024-1
Health Professional from TAIWAN, PROVINCE OF CHINA reported METFORMIN problem on Nov 20, 2007. Female patient was diagnosed with type 2 diabetes mellitus and was treated with METFORMIN. After drug was administered, patient experienced the following problems/side effects: anaemia megaloblastic, deep vein thrombosis, hyperhomocysteinaemia, vitamin b12 deficiency, . METFORMIN dosage: 500 MG, BID. During the same period patient was treated with GLYBURIDE, INSULIN, VITAMIN B. Patient was hospitalized. Patient recovered.

Metformin Side Effects Report #5537080-6
METFORMIN problem was reported by a Health Professional from GERMANY on Dec 05, 2007. Female patient, 65 years of age, was diagnosed with type 2 diabetes mellitus and was treated with METFORMIN. After drug was administered, patient experienced the following problems/side effects: anaemia megaloblastic, cervicobrachial syndrome, deep vein thrombosis, hyperhomocysteinaemia, vitamin b12 deficiency, . METFORMIN dosage: unknown. During the same period patient was treated with PYRIDOSTIGMINE BROMIDE, GLYBURIDE. Patient was hospitalized. Patient recovered.

Viramune Side Effects Report #5547642-8
Physician from GERMANY reported VIRAMUNE problem on Dec 04, 2007. Male patient was diagnosed with hiv infection and was treated with VIRAMUNE. After drug was administered, patient experienced the following problems/side effects: anaemia megaloblastic, . VIRAMUNE dosage: unknown. During the same period patient was treated with COMBIVIR, HALDOL. Patient was hospitalized. Patient recovered.

Metformin Side Effects Report #5552088-2
METFORMIN problem was reported by a Consumer or non-health professional from TAIWAN, PROVINCE OF CHINA on Nov 25, 2007. Female patient, 65 years of age, was diagnosed with type 2 diabetes mellitus and was treated with METFORMIN. After drug was administered, patient experienced the following problems/side effects: anaemia megaloblastic, asthenia, blood lactate dehydrogenase increased, cervicobrachial syndrome, deep vein thrombosis, dyspnoea exertional, hyperhomocysteinaemia, vitamin b12 deficiency, . METFORMIN dosage: 500 MG; TWICE A DAY. During the same period patient was treated with GLYBURIDE. Patient was hospitalized. Patient recovered.

Combivir Side Effects Report #5564988-8
Physician from GERMANY reported COMBIVIR problem on Dec 17, 2007. Male patient, 26 years of age, weighting 172.0 lb, was diagnosed with hiv infection and was treated with COMBIVIR. After drug was administered, patient experienced the following problems/side effects: anaemia megaloblastic, . COMBIVIR dosage: unknown. During the same period patient was treated with VIRAMUNE, HALDOL. Patient recovered.


Viramune Side Effects Report #5572005-9
VIRAMUNE problem was reported by a Physician from GERMANY on Dec 13, 2007. Male patient, weighting 172.0 lb, was diagnosed with hiv infection, schizophrenia and was treated with VIRAMUNE. After drug was administered, patient experienced the following problems/side effects: anaemia megaloblastic, . VIRAMUNE dosage: unknown. During the same period patient was treated with COMBIVIR, HALDOL. Patient was hospitalized. Patient recovered.

Metformin Side Effects Report #5574503-0
Health Professional from TAIWAN, PROVINCE OF CHINA reported METFORMIN problem on Dec 17, 2007. Female patient was diagnosed with type 2 diabetes mellitus and was treated with METFORMIN. After drug was administered, patient experienced the following problems/side effects: anaemia megaloblastic, deep vein thrombosis, hyperhomocysteinaemia, vitamin b12 deficiency, . METFORMIN dosage: 500 MG, BID. During the same period patient was treated with GLYBURIDE, INSULIN, VITAMIN B. Patient was hospitalized. Patient recovered.

Losec Side Effects Report #5508726-3
LOSEC problem was reported by a Physician from EGYPT on Nov 06, 2007. Male patient, weighting 176.4 lb, was diagnosed with ulcer, prostate cancer, cardiovascular disorder and was treated with LOSEC. After drug was administered, patient experienced the following problems/side effects: anaemia megaloblastic, asthenia, chromaturia, depression, dizziness, dyspnoea, haemolytic anaemia, jaundice, polyuria, . LOSEC dosage: unknown. During the same period patient was treated with ZOLADEX, OXYBRAL, BUMETANIDE, ALDACTONE, SOLUPRED, MISOTEC, DAKTARIN, MYCOSTATIN. Patient was hospitalized. Patient recovered.

Metformin Side Effects Report #5515849-1
Health Professional from GERMANY reported METFORMIN problem on Nov 05, 2007. Female patient, 65 years of age, was diagnosed with diabetes mellitus and was treated with METFORMIN. After drug was administered, patient experienced the following problems/side effects: anaemia megaloblastic, deep vein thrombosis, hyperhomocysteinaemia, vitamin b12 deficiency, . METFORMIN dosage: unknown. Patient recovered.

Metformin Side Effects Report #5520808-9
METFORMIN problem was reported by a Health Professional from GERMANY on Nov 09, 2007. Female patient, 65 years of age, was diagnosed with type 2 diabetes mellitus and was treated with METFORMIN. After drug was administered, patient experienced the following problems/side effects: anaemia megaloblastic, deep vein thrombosis, hyperhomocysteinaemia, vitamin b12 deficiency, . METFORMIN dosage: unknown. During the same period patient was treated with GLYBURIDE. Patient was hospitalized. Patient recovered.


Actos Side Effects Report #5526100-0
Consumer or non-health professional from GREECE reported ACTOS problem on Nov 13, 2007. Male patient, 76 years of age, was diagnosed with type 2 diabetes mellitus and was treated with ACTOS. After drug was administered, patient experienced the following problems/side effects: anaemia megaloblastic, . ACTOS dosage: 30 MG (30 MG, 1 IN 1 D) PER ORAL. During the same period patient was treated with ANTIHYPERTENSIVES, METFORMIN. Patient recovered.

Metformin Side Effects Report #5526616-7
METFORMIN problem was reported by a Health Professional from GERMANY on Nov 26, 2007. Female patient, 65 years of age, was diagnosed with type 2 diabetes mellitus and was treated with METFORMIN. After drug was administered, patient experienced the following problems/side effects: anaemia megaloblastic, blood lactate dehydrogenase increased, deep vein thrombosis, fibrin d dimer increased, gene mutation, hyperhomocysteinaemia, hypoaesthesia, vitamin b12 deficiency, . METFORMIN dosage: unknown. During the same period patient was treated with GLYBURIDE. Patient was hospitalized. Patient recovered.

Fortamet Side Effects Report #5528413-5
Health Professional from TAIWAN, PROVINCE OF CHINA reported FORTAMET problem on Nov 13, 2007. Female patient, 65 years of age, was diagnosed with type 2 diabetes mellitus and was treated with FORTAMET. After drug was administered, patient experienced the following problems/side effects: anaemia megaloblastic, deep vein thrombosis, hyperhomocysteinaemia, vitamin b12 deficiency, . FORTAMET dosage: 500 MG, BID. During the same period patient was treated with GLYBURIDE, PYRIDOSTIGMINE. Patient was hospitalized. Patient recovered.

Raptiva Side Effects Report #5528982-5
RAPTIVA problem was reported by a Physician from SWITZERLAND on Nov 26, 2007. Female patient, 42 years of age, was diagnosed with psoriasis, ear infection and was treated with RAPTIVA. After drug was administered, patient experienced the following problems/side effects: anaemia megaloblastic, fatigue, pancytopenia, . RAPTIVA dosage: unknown. During the same period patient was treated with PENICILLIN G, CLINDAMYCIN, CEFAMANDOLE. Patient was hospitalized. Patient recovered.

Actos Side Effects Report #5486011-6
Consumer or non-health professional from GREECE reported ACTOS problem on Oct 08, 2007. Male patient, 76 years of age, was diagnosed with type 2 diabetes mellitus and was treated with ACTOS. After drug was administered, patient experienced the following problems/side effects: anaemia megaloblastic, . ACTOS dosage: 30 MG (30 MG, 1 IN 1 D), PER ORAL. During the same period patient was treated with ANTIHYPERTENSIVES, METFORMIN. Patient recovered.


Strattera Side Effects Report #5441831-9
STRATTERA problem was reported by a Physician from UNITED STATES on Aug 23, 2007. Male patient, 16 years of age, was diagnosed with attention deficit/hyperactivity disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: anaemia megaloblastic, platelet count decreased, road traffic accident, white blood cell count decreased, . STRATTERA dosage: unknown. Patient recovered.

Avandamet Side Effects Report #5407231-2
Consumer or non-health professional from UNITED STATES reported AVANDAMET problem on Aug 02, 2007. Female patient, 72 years of age, was treated with AVANDAMET. After drug was administered, patient experienced the following problems/side effects: anaemia megaloblastic, pancytopenia, . AVANDAMET dosage: unknown. Patient recovered.

Aricept Side Effects Report #5411263-8
ARICEPT problem was reported by a Pharmacist from JAPAN on Aug 03, 2007. Female patient, 73 years of age, weighting 66.91 lb, was diagnosed with dementia alzheimer's type and was treated with ARICEPT. After drug was administered, patient experienced the following problems/side effects: anaemia megaloblastic, anaemia vitamin b12 deficiency, condition aggravated, leukopenia, . ARICEPT dosage: 2.5 MG, 1 IN 1 D, ORAL. Patient was hospitalized. Patient recovered.

Malarone Side Effects Report #5757075-7
Consumer or non-health professional from FRANCE reported MALARONE problem on May 21, 2008. Female patient, 36 years of age, was diagnosed with plasmodium falciparum infection and was treated with MALARONE. After drug was administered, patient experienced the following problems/side effects: anaemia megaloblastic, asthenia, epistaxis, haemorrhage, nausea, pancytopenia, vomiting, . MALARONE dosage: unknown. During the same period patient was treated with IVERMECTIN. Patient was hospitalized. Patient recovered.

Effexor Side Effects Report #5701048-7
EFFEXOR problem was reported by a Health Professional from FRANCE on Apr 03, 2008. Female patient, weighting 152.1 lb, was diagnosed with depression and was treated with EFFEXOR. After drug was administered, patient experienced the following problems/side effects: anaemia megaloblastic, antinuclear antibody positive, bone marrow failure, erythroblastosis, haptoglobin decreased, . EFFEXOR dosage: unknown. During the same period patient was treated with LEVOTHYROXINE, PIASCLEDINE, BROMAZEPAM, PARACETAMOL. Patient was hospitalized. Patient recovered.

Cisplatin Side Effects Report #5714808-3
Consumer or non-health professional from IRELAND reported CISPLATIN problem on Apr 22, 2008. Female patient, 61 years of age, was diagnosed with gastric cancer, hypertension, ulcer, mineral supplementation, sedation and was treated with CISPLATIN. After drug was administered, patient experienced the following problems/side effects: anaemia megaloblastic, . CISPLATIN dosage: unknown. During the same period patient was treated with LOSARTAN POTASSIUM, BISOPROLOL FUMARATE, PEPTORAN, FERRUM, HELEX. Patient was hospitalized. Patient recovered.

Arava Side Effects Report #5342007-6
ARAVA problem was reported by a Physician from CZECH REPUBLIC on May 28, 2007. Male patient, 62 years of age, was diagnosed with rheumatoid arthritis, gastritis, hypercholesterolaemia and was treated with ARAVA. After drug was administered, patient experienced the following problems/side effects: anaemia megaloblastic, aortic stenosis, atrial fibrillation, basophil count increased, cardiac aneurysm, cardiac failure, circulatory collapse, dilatation ventricular, dyspnoea, . ARAVA dosage: unknown. During the same period patient was treated with METHOTREXATE, MEDROL, HELICID, SORTIS, POTASSIUM CHLORIDE, VIGANTOL. Patient was hospitalized. Patient recovered.

Arava Side Effects Report #5336645-4
Physician from CZECH REPUBLIC reported ARAVA problem on May 21, 2007. Male patient, 62 years of age, was diagnosed with rheumatoid arthritis, gastritis, hypercholesterolaemia and was treated with ARAVA. After drug was administered, patient experienced the following problems/side effects: anaemia megaloblastic, atrial fibrillation, cardiac failure, circulatory collapse, dyspnoea, infection, pulmonary oedema, syncope, . ARAVA dosage: unknown. During the same period patient was treated with METHOTREXATE, MEDROL, HELICID, SORTIS, POTASSIUM CHLORIDE, VIGANTOL. Patient was hospitalized. Patient recovered.

Arava Side Effects Report #5303033-6
ARAVA problem was reported by a Physician from CZECH REPUBLIC on Apr 12, 2007. Male patient, 62 years of age, was diagnosed with rheumatoid arthritis, gastritis and was treated with ARAVA. After drug was administered, patient experienced the following problems/side effects: anaemia megaloblastic, circulatory collapse, . ARAVA dosage: unknown. During the same period patient was treated with METHOTREXATE, MEDROL, HELICID, SORTIS, POTASSIUM CHLORIDE, VIGANTOL, CALCIUM EFFERVESCENT. Patient was hospitalized. Patient recovered.

Arava Side Effects Report #5259848-6
Physician from SOUTH AFRICA reported ARAVA problem on Mar 06, 2007. Female patient, 64 years of age, was diagnosed with rheumatoid arthritis, menopause, hypertension and was treated with ARAVA. After drug was administered, patient experienced the following problems/side effects: anaemia megaloblastic, mycobacterial infection, myelofibrosis, . ARAVA dosage: unknown. During the same period patient was treated with METHOTREXATE, ACTIVELLE, DYNACIRC, FOLIC ACID, CELEBREX, NEXIAM. Patient recovered.

Metformin Side Effects Report #5603425-1
METFORMIN problem was reported by a Physician from TAIWAN, PROVINCE OF CHINA on Jan 07, 2008. Female patient, 65 years of age, was diagnosed with type 2 diabetes mellitus and was treated with METFORMIN. After drug was administered, patient experienced the following problems/side effects: anaemia macrocytic, anaemia megaloblastic, blood lactate dehydrogenase increased, cervicobrachial syndrome, deep vein thrombosis, hyperhomocysteinaemia, hypoaesthesia, myasthenia gravis, thymoma, . METFORMIN dosage: 500 MG TWICE DAILY. During the same period patient was treated with GLYBURIDE. Patient was hospitalized. Patient recovered.

Accutane Side Effects Report #5571862-X
Consumer or non-health professional from UNITED STATES reported ACCUTANE problem on Dec 11, 2007. Female patient, child 12 years of age, weighting 145.1 lb, was treated with ACCUTANE. After drug was administered, patient experienced the following problems/side effects: agitation, anaemia megaloblastic, anal fissure, aortic valve incompetence, aphasia, autoimmune disorder, benign intracranial hypertension, cervicobrachial syndrome, clumsiness, . ACCUTANE dosage: unknown. Patient was hospitalized and became disabled. Patient recovered.

Combivir Side Effects Report #5574982-9
COMBIVIR problem was reported by a Consumer or non-health professional from FRANCE on Dec 18, 2007. Male patient, 42 years of age, was diagnosed with toxoplasma serology positive and was treated with COMBIVIR. After drug was administered, patient experienced the following problems/side effects: anaemia macrocytic, anaemia megaloblastic, folate deficiency, haematotoxicity, vitamin b12 deficiency, . COMBIVIR dosage: unknown. During the same period patient was treated with BACTRIM DS, KALETRA, IMOVANE, BICARBONATE. Patient was hospitalized. Patient recovered.

Accutane Side Effects Report #5738506-5
Consumer or non-health professional from UNITED STATES reported ACCUTANE problem on May 01, 2008. Female patient, weighting 145.1 lb, was treated with ACCUTANE. After drug was administered, patient experienced the following problems/side effects: agitation, anaemia megaloblastic, anal fissure, aortic valve incompetence, aphasia, autoimmune disorder, benign intracranial hypertension, cervicobrachial syndrome, clumsiness, . ACCUTANE dosage: unknown. Patient was hospitalized and became disabled. Patient recovered.

Accutane Side Effects Report #5748917-X
ACCUTANE problem was reported by a Consumer or non-health professional from UNITED STATES on May 15, 2008. Female patient, weighting 145.1 lb, was treated with ACCUTANE. After drug was administered, patient experienced the following problems/side effects: agitation, anaemia megaloblastic, anal fissure, aortic valve incompetence, aphasia, autoimmune disorder, benign intracranial hypertension, cervicobrachial syndrome, clumsiness, . ACCUTANE dosage: unknown. Patient was hospitalized and became disabled. Patient recovered.

Metformin Side Effects Report #5718991-5
Physician from TAIWAN, PROVINCE OF CHINA reported METFORMIN HYDROCHLORIDE problem on Apr 09, 2008. Female patient, 65 years of age, was diagnosed with type 2 diabetes mellitus and was treated with METFORMIN HYDROCHLORIDE. After drug was administered, patient experienced the following problems/side effects: anaemia macrocytic, anaemia megaloblastic, blood lactate dehydrogenase increased, cervicobrachial syndrome, deep vein thrombosis, fibrin d dimer increased, gene mutation, hyperhomocysteinaemia, hypoaesthesia, . METFORMIN HYDROCHLORIDE dosage: 500 MG;BID. During the same period patient was treated with GLYBURIDE, PYRIDOSTIGMINE BROMIDE. Patient was hospitalized. Patient recovered.

Accutane Side Effects Report #5374230-9
ACCUTANE problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 15, 2007. Female patient, child 12 years of age, weighting 145.1 lb, was treated with ACCUTANE. After drug was administered, patient experienced the following problems/side effects: agitation, anaemia megaloblastic, anal fissure, aortic valve incompetence, autoimmune disorder, benign intracranial hypertension, cervicobrachial syndrome, colitis ulcerative, confusional state, . ACCUTANE dosage: unknown. Patient was hospitalized and became disabled. Patient recovered.

Accutane Side Effects Report #5278118-3
Consumer or non-health professional from UNITED STATES reported ACCUTANE problem on Mar 15, 2007. Female patient, child 12 years of age, weighting 145.1 lb, was treated with ACCUTANE. After drug was administered, patient experienced the following problems/side effects: agitation, anaemia megaloblastic, anal fissure, aortic valve incompetence, autoimmune disorder, benign intracranial hypertension, cervicobrachial syndrome, colitis ulcerative, confusional state, . ACCUTANE dosage: unknown. Patient was hospitalized and became disabled. Patient recovered.