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ASPIRATION BONE MARROW side effect

What is ASPIRATION BONE MARROW ?
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Drugs associated with ASPIRATION BONE MARROW

AZATHIOPRINE  EXJADE  LAMISIL  NSAID  TARGOCID  VOLTAREN  


Targocid Side Effects Report #5641066-0
Consumer or non-health professional from reported TARGOCID problem on Feb 18, 2008. Female patient, 77 years of age, was treated with TARGOCID. After drug was administered, patient experienced the following problems/side effects: aspiration bone marrow, bone marrow failure, erythropenia, leukopenia, pancytopenia, thrombocytopenia, . TARGOCID dosage: unknown. During the same period patient was treated with RIFADIN, SECTRAL, METOCLOPRAMIDE, AMLOR, HYZAAR. Patient was hospitalized. Patient recovered.

Targocid Side Effects Report #5528349-X
TARGOCID problem was reported by a Consumer or non-health professional from on Nov 19, 2007. Female patient, 77 years of age, was diagnosed with staphylococcal sepsis and was treated with TARGOCID. After drug was administered, patient experienced the following problems/side effects: aspiration bone marrow, bone marrow failure, erythropenia, leukopenia, pancytopenia, thrombocytopenia, . TARGOCID dosage: unknown. During the same period patient was treated with RIFADIN, SECTRAL, METOCLOPRAMIDE, AMLOR, HYZAAR. Patient was hospitalized. Patient recovered.

Targocid Side Effects Report #5491957-9
Consumer or non-health professional from reported TARGOCID problem on Oct 10, 2007. Female patient, 77 years of age, was treated with TARGOCID. After drug was administered, patient experienced the following problems/side effects: aspiration bone marrow, bone marrow failure, erythropenia, leukopenia, pancytopenia, thrombocytopenia, . TARGOCID dosage: unknown. During the same period patient was treated with RIFADIN, SECTRAL, PRIMPERAN, AMLOR, HYZAAR. Patient was hospitalized. Patient recovered.

Lamisil Side Effects Report #5377518-0
LAMISIL problem was reported by a Physician from JAPAN on June 26, 2007. Female patient, 77 years of age, was diagnosed with nail tinea, hyperlipidaemia, hypertension and was treated with LAMISIL. After drug was administered, patient experienced the following problems/side effects: aspiration bone marrow, blood immunoglobulin g increased, haemorrhage subcutaneous, idiopathic thrombocytopenic purpura, . LAMISIL dosage: 125 MG/DAY. During the same period patient was treated with LIPITOR, ADALAT. Patient recovered.


Lamisil Side Effects Report #5377518-0
Physician from JAPAN reported LAMISIL problem on June 26, 2007. Female patient, 77 years of age, was diagnosed with nail tinea, hyperlipidaemia, hypertension and was treated with LAMISIL. After drug was administered, patient experienced the following problems/side effects: aspiration bone marrow, blood immunoglobulin g increased, haemorrhage subcutaneous, idiopathic thrombocytopenic purpura, . LAMISIL dosage: 125 MG/DAY. During the same period patient was treated with LIPITOR, ADALAT. Patient recovered.

Targocid Side Effects Report #5789443-1
TARGOCID problem was reported by a Consumer or non-health professional from on Feb 18, 2008. Female patient, 77 years of age, was treated with TARGOCID. After drug was administered, patient experienced the following problems/side effects: aspiration bone marrow, bone marrow failure, erythropenia, leukopenia, pancytopenia, thrombocytopenia, . TARGOCID dosage: unknown. During the same period patient was treated with RIFADIN, SECTRAL, PRIMPERAN, AMLOR, HYZAAR. Patient was hospitalized. Patient recovered.

Lamisil Side Effects Report #5276819-4
Physician from JAPAN reported LAMISIL problem on Mar 15, 2007. Female patient, 77 years of age, was diagnosed with nail tinea, hyperlipidaemia, hypertension and was treated with LAMISIL. After drug was administered, patient experienced the following problems/side effects: aspiration bone marrow, blood immunoglobulin g increased, haemorrhage subcutaneous, idiopathic thrombocytopenic purpura, . LAMISIL dosage: 125 MG/DAY. During the same period patient was treated with LIPITOR, ADALAT. Patient recovered.

Nsaid Side Effects Report #5739219-6
NSAID problem was reported by a Consumer or non-health professional from JAPAN on May 08, 2008. Female patient, 76 years of age, was diagnosed with angina pectoris, cerebral infarction and was treated with NSAID. After drug was administered, patient experienced the following problems/side effects: angina pectoris, aspiration bone marrow, endoscopy, fatigue, gastric ulcer, iron deficiency anaemia, mucosal inflammation, oedema mucosal, small intestine ulcer, . NSAID dosage: unknown. During the same period patient was treated with ASPIRIN, DICLOFENAC. Patient recovered.

Azathioprine Side Effects Report #5740375-4
Health Professional from ITALY reported AZATHIOPRINE problem on May 02, 2008. Male patient, 67 years of age, was diagnosed with immunosuppression and was treated with AZATHIOPRINE. After drug was administered, patient experienced the following problems/side effects: abdominal pain, aspiration bone marrow, b-cell lymphoma, blood alkaline phosphatase increased, blood lactate dehydrogenase increased, bone marrow necrosis, bone pain, night sweats, normochromic normocytic anaemia, . AZATHIOPRINE dosage: unknown. During the same period patient was treated with PREDNISONE, CYCLOSPORINE. Patient was hospitalized. Patient recovered.


Voltaren Side Effects Report #5751640-9
VOLTAREN problem was reported by a Health Professional from JAPAN on May 20, 2008. Female patient, 76 years of age, was diagnosed with cerebral infarction, angina pectoris and was treated with VOLTAREN. After drug was administered, patient experienced the following problems/side effects: angina pectoris, aspiration bone marrow, endoscopy, fatigue, gastric ulcer, iron deficiency anaemia, mucosal inflammation, oedema mucosal, small intestine ulcer, . VOLTAREN dosage: unknown. During the same period patient was treated with NSAID, ASPIRIN, MELOXICAM. Patient recovered.

Exjade Side Effects Report #5262213-9
Physician from CANADA reported EXJADE problem on Feb 26, 2007. Male patient, 66 years of age, was diagnosed with iron overload and was treated with EXJADE. After drug was administered, patient experienced the following problems/side effects: alanine aminotransferase increased, aspartate aminotransferase increased, aspiration bone marrow, biopsy bone marrow abnormal, blood bilirubin increased, blood creatinine increased, blood glucose increased, blood iron increased, blood sodium decreased, . EXJADE dosage: 2500 MG, QD. During the same period patient was treated with DESFERAL, ENOXAPARIN, WARFARIN, LOSARTAN POSTASSIUM, DIGOXIN, DOFETILIDE, DUTASTERIDE, ASCORBIC ACID. Patient recovered.

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