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BONE MARROW MYELOGRAM ABNORMAL side effect

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Byetta Side Effects Report #5653173-7
Physician from UNITED STATES reported BYETTA problem on Oct 03, 2007. Male patient, 52 years of age, was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: bone marrow myelogram abnormal, haemoglobin decreased, white blood cell count, . BYETTA dosage: unknown. During the same period patient was treated with ACTOS. Patient recovered.

Feldene Side Effects Report #5487486-9
FELDENE problem was reported by a Consumer or non-health professional from BRAZIL on Oct 04, 2007. Male patient, weighting 136.7 lb, was diagnosed with headache, eye pain and was treated with FELDENE. After drug was administered, patient experienced the following problems/side effects: bone marrow myelogram abnormal, prothrombin time abnormal, thrombocytopenia, . FELDENE dosage: unknown. Patient was hospitalized. Patient recovered.

Cyclosporine Side Effects Report #5371647-3
Consumer or non-health professional from FRANCE reported CYCLOSPORINE problem on June 25, 2007. Male patient, 47 years of age, was diagnosed with liver transplant and was treated with CYCLOSPORINE. After drug was administered, patient experienced the following problems/side effects: bone marrow myelogram abnormal, oedema peripheral, pancytopenia, pseudomonas infection, rash, renal failure, . CYCLOSPORINE dosage: 175 MG DAILY. During the same period patient was treated with ALLOPURINOL, DELURSAN, ASPEGIC, AZATHIOPRINE, CERTICAN. Patient was hospitalized. Patient recovered.

Nicardipine Side Effects Report #5297426-3
NICARDIPINE HYDROCHLORIDE problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Mar 26, 2007. Female patient, 65 years of age, was treated with NICARDIPINE HYDROCHLORIDE. After drug was administered, patient experienced the following problems/side effects: bone marrow myelogram abnormal, granulocytes abnormal, histiocytosis haematophagic, leukopenia, multiple injuries, neutropenia, pneumothorax, . NICARDIPINE HYDROCHLORIDE dosage: unknown. During the same period patient was treated with ACUPAN, LORAZEPAM, VENLAFAXINE, ESOMEPRAZOLE, ACETAMINOPHEN. Patient recovered.


Augmentin Side Effects Report #5704430-7
Consumer or non-health professional from FRANCE reported AUGMENTIN problem on Apr 04, 2008. Male patient, 78 years of age, was diagnosed with febrile infection and was treated with AUGMENTIN. After drug was administered, patient experienced the following problems/side effects: anaemia, bone marrow myelogram abnormal, erythropoiesis abnormal, haemoglobin decreased, neutrophil count decreased, pancytopenia, platelet count decreased, red blood cell count decreased, thrombocytopenia, . AUGMENTIN dosage: unknown. During the same period patient was treated with XATRAL, PROSCAR, TOPALGIC, CALCIPARINE, COZAAR, PLAVIX, OMEPRAZOLE, ALPRAZOLAM. Patient was hospitalized. Patient recovered.

Depakene Side Effects Report #5316518-3
DEPAKENE problem was reported by a Health Professional from FRANCE on Apr 25, 2007. Male patient, 41 years of age, was diagnosed with myoclonic epilepsy, head injury and was treated with DEPAKENE. After drug was administered, patient experienced the following problems/side effects: anisocytosis, bone marrow myelogram abnormal, convulsion, essential thrombocythaemia, leukocytosis, platelet morphology abnormal, . DEPAKENE dosage: unknown. During the same period patient was treated with CLONAZEPAM, DIAZEPAM, OXCARBAZEPINE. Patient was hospitalized. Patient recovered.