EOSINOPHIL COUNT DECREASED side effect
What is EOSINOPHIL COUNT DECREASED ?
Help Community - Describe Your Side Effect
Search FDA Side Effects
Ask Health Expert
EOSINOPHIL COUNT DECREASED and Recently Reported Side Effects
EOSINOPHIL COUNT DECREASED and 15 most Active Side Effect polls
EOSINOPHIL COUNT DECREASED and featured health surveys
Substances toxic to Health
Recent Hospital reviews
Comments about Side Effects
Hospital Quality reviews
Homecare Quality reviews
Drugs associated with EOSINOPHIL COUNT DECREASED
ARIXTRA AUGMENTIN CEFAMEZIN CLOZARIL COMTAN CONCERTA EFFEXOR HORMONAL MEIACT OFLOCET PAXIL YASMIN ZADITOR ZIDOVUDINE ZOLADEXMeiact Side Effects Report #5558115-0
Consumer or non-health professional from JAPAN reported MEIACT problem on Nov 30, 2007. Male patient, 39 years of age, was diagnosed with nasopharyngitis and was treated with MEIACT. After drug was administered, patient experienced the following problems/side effects: eosinophil count decreased, erythema, gait disturbance, pain in extremity, purpura, toxic skin eruption, viral infection, . MEIACT dosage: 300 MG, PO. During the same period patient was treated with CONFATANIN, ALUSA. Patient recovered.
Cefamezin Side Effects Report #5453891-X
CEFAMEZIN problem was reported by a Pharmacist from JAPAN on Sept 12, 2007. Male patient, 64 years of age, was treated with CEFAMEZIN. After drug was administered, patient experienced the following problems/side effects: eosinophil count decreased, platelet count decreased, white blood cell count increased, . CEFAMEZIN dosage: unknown. During the same period patient was treated with LANSOPRAZOLE, ACECOL, AMLODIPINE, LIVALO, FLIVAS. Patient was hospitalized. Patient recovered.
Cefamezin Side Effects Report #5464294-6
Pharmacist from JAPAN reported CEFAMEZIN problem on Sept 18, 2007. Male patient, 64 years of age, was treated with CEFAMEZIN. After drug was administered, patient experienced the following problems/side effects: eosinophil count decreased, laboratory test interference, platelet count decreased, white blood cell count increased, . CEFAMEZIN dosage: unknown. During the same period patient was treated with LANSOPRAZOLE, ACECOL, AMLODIPINE, LIVALO, FLIVAS. Patient was hospitalized. Patient recovered.
Arixtra Side Effects Report #5775208-3
ARIXTRA problem was reported by a Physician from JAPAN on June 12, 2008. Male patient, 77 years of age, weighting 125.7 lb, was diagnosed with thrombosis prophylaxis, infection prophylaxis, analgesia and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: eosinophil count decreased, haematocrit decreased, haemoglobin decreased, interstitial lung disease, lymphocyte count decreased, neutrophil count increased, pulmonary alveolar haemorrhage, red blood cell count decreased, respiratory disorder, . ARIXTRA dosage: 2.5MG PER DAY. During the same period patient was treated with SULPERAZON, LOXONIN, MUCOSTA, CEFAMEZIN. Patient was hospitalized. Patient recovered.
Comtan Side Effects Report #5726218-3
Physician from JAPAN reported COMTAN problem on Apr 25, 2008. Female patient, 80 years of age, was diagnosed with parkinsonian gait, parkinson's disease, constipation, pain in extremity and was treated with COMTAN. After drug was administered, patient experienced the following problems/side effects: eosinophil count decreased, leukopenia, monocyte count decreased, myelodysplastic syndrome, nausea, pain in extremity, platelet count decreased, white blood cell count decreased, . COMTAN dosage: 100MG/TID. During the same period patient was treated with LEVODOPA, PRAMIPEXOLE DIHYDROCHLORIDE, MAGMITT KENEI, MOBIC, MUCOSTA, SELEGILINE HYDROCHLORIDE. Patient recovered.
Arixtra Side Effects Report #5737733-0
ARIXTRA problem was reported by a Physician from JAPAN on May 12, 2008. Male patient, 77 years of age, weighting 125.7 lb, was diagnosed with thrombosis prophylaxis, infection prophylaxis, analgesia and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: eosinophil count decreased, haematocrit decreased, haemoglobin decreased, interstitial lung disease, lymphocyte count decreased, neutrophil count increased, pulmonary alveolar haemorrhage, red blood cell count decreased, white blood cell count increased, . ARIXTRA dosage: 2.5MG PER DAY. During the same period patient was treated with SULPERAZON, LOXONIN, MUCOSTA, CEFAMEZIN. Patient was hospitalized. Patient recovered.
Yasmin Side Effects Report #5697064-4
Physician from UNITED STATES reported YASMIN problem on June 08, 2007. Female patient, 26 years of age, weighting 160.9 lb, was diagnosed with oral contraception, multiple allergies and was treated with YASMIN. After drug was administered, patient experienced the following problems/side effects: eosinophil count decreased, fatigue, . YASMIN dosage: unknown. During the same period patient was treated with MIRALAX, ZADITOR. Patient recovered.
Yasmin Side Effects Report #5354520-6
YASMIN problem was reported by a Health Professional from UNITED STATES on June 08, 2007. Female patient, 26 years of age, weighting 160.9 lb, was diagnosed with oral contraception, multiple allergies and was treated with YASMIN. After drug was administered, patient experienced the following problems/side effects: eosinophil count decreased, fatigue, . YASMIN dosage: unknown. During the same period patient was treated with MIRALAX, ZADITOR. Patient recovered.
Hormonal Side Effects Report #5360166-6
Physician from UNITED STATES reported HORMONAL CONTRACEPTIVES problem on June 07, 2007. Female patient, 26 years of age, weighting 160.0 lb, was diagnosed with contraception, eye allergy and was treated with HORMONAL CONTRACEPTIVES. After drug was administered, patient experienced the following problems/side effects: eosinophil count decreased, . HORMONAL CONTRACEPTIVES dosage: unknown. During the same period patient was treated with ZADITOR. Patient recovered.
Yasmin Side Effects Report #5306241-3
YASMIN problem was reported by a Physician from UNITED STATES on Apr 13, 2007. Female patient, 26 years of age, weighting 160.9 lb, was treated with YASMIN. After drug was administered, patient experienced the following problems/side effects: eosinophil count decreased, fatigue, . YASMIN dosage: unknown. During the same period patient was treated with MIRALAX. Patient recovered.
Zaditor Side Effects Report #5308124-1
Physician from UNITED STATES reported ZADITOR problem on Apr 16, 2007. Female patient, 26 years of age, was treated with ZADITOR. After drug was administered, patient experienced the following problems/side effects: eosinophil count decreased, . ZADITOR dosage: unknown. During the same period patient was treated with HORMONAL CONTRACEPTIVES. Patient recovered.
Zoladex Side Effects Report #5264498-1
ZOLADEX problem was reported by a Consumer or non-health professional from BRAZIL on Mar 07, 2007. Female patient, 32 years of age, weighting 110.2 lb, was diagnosed with endometriosis, hypertension and was treated with ZOLADEX. After drug was administered, patient experienced the following problems/side effects: eosinophil count decreased, lymphocyte count decreased, neutrophil count decreased, white blood cell count decreased, . ZOLADEX dosage: unknown. During the same period patient was treated with VASOPRIL. Patient recovered.
Concerta Side Effects Report #5551239-3
Physician from SWEDEN reported CONCERTA problem on Dec 03, 2007. Male patient, child 9 years of age, was diagnosed with attention deficit/hyperactivity disorder and was treated with CONCERTA. After drug was administered, patient experienced the following problems/side effects: anorexia, eosinophil count decreased, . CONCERTA dosage: unknown. During the same period patient was treated with MELATONIN, RITALIN. Patient recovered.
Paxil Side Effects Report #5525539-7
PAXIL problem was reported by a Physician from JAPAN on Nov 20, 2007. Female patient, 83 years of age, weighting 83.78 lb, was diagnosed with dementia alzheimer's type and was treated with PAXIL. After drug was administered, patient experienced the following problems/side effects: bleeding time prolonged, eosinophil count decreased, epistaxis, fatigue, haematocrit decreased, malaise, monocyte count increased, neutrophil count increased, pancytopenia, . PAXIL dosage: unknown. During the same period patient was treated with GRAMALIL, RISPERDAL. Patient was hospitalized. Patient recovered.
Paxil Side Effects Report #5382976-1
Physician from JAPAN reported PAXIL problem on July 05, 2007. Female patient, 83 years of age, weighting 83.78 lb, was diagnosed with dementia alzheimer's type and was treated with PAXIL. After drug was administered, patient experienced the following problems/side effects: bleeding time prolonged, eosinophil count decreased, epistaxis, fatigue, haematocrit decreased, malaise, monocyte count increased, neutrophil count increased, pancytopenia, . PAXIL dosage: 25MG PER DAY. During the same period patient was treated with GRAMALIL, RISPERDAL. Patient was hospitalized. Patient recovered.
Paxil Side Effects Report #5382976-1
PAXIL problem was reported by a Physician from JAPAN on July 05, 2007. Female patient, 83 years of age, weighting 83.78 lb, was diagnosed with dementia alzheimer's type and was treated with PAXIL. After drug was administered, patient experienced the following problems/side effects: bleeding time prolonged, eosinophil count decreased, epistaxis, fatigue, haematocrit decreased, malaise, monocyte count increased, neutrophil count increased, pancytopenia, . PAXIL dosage: 25MG PER DAY. During the same period patient was treated with GRAMALIL, RISPERDAL. Patient was hospitalized. Patient recovered.
Oflocet Side Effects Report #5762868-6
Health Professional from JAPAN reported OFLOCET problem on May 29, 2008. Male patient, 62 years of age, weighting 405.7 lb, was diagnosed with prostatitis, erysipelas, gastric ulcer and was treated with OFLOCET. After drug was administered, patient experienced the following problems/side effects: agranulocytosis, eosinophil count decreased, haemoglobin decreased, leukopenia, thrombocytopenia, . OFLOCET dosage: unknown. During the same period patient was treated with AUGMENTIN, RABEPRAZOLE, ZOLOFT, AVLOCARDYL, VITAMINS B1 AND B6. Patient was hospitalized. Patient recovered.
Augmentin Side Effects Report #5707052-7
AUGMENTIN problem was reported by a Consumer or non-health professional from FRANCE on Apr 02, 2008. Male patient, 62 years of age, was diagnosed with erysipelas, prostatitis and was treated with AUGMENTIN. After drug was administered, patient experienced the following problems/side effects: agranulocytosis, eosinophil count decreased, haemoglobin decreased, leukopenia, neutrophil percentage decreased, platelet count decreased, . AUGMENTIN dosage: unknown. During the same period patient was treated with OFLOCET, PARIET, ZOLOFT, AVLOCARDYL, VIT B. Patient was hospitalized. Patient recovered.
Oflocet Side Effects Report #5717852-5
Health Professional from FRANCE reported OFLOCET problem on Apr 15, 2008. Male patient, 62 years of age, was diagnosed with prostatitis, erysipelas, gastric ulcer and was treated with OFLOCET. After drug was administered, patient experienced the following problems/side effects: agranulocytosis, eosinophil count decreased, haemoglobin decreased, leukopenia, thrombocytopenia, . OFLOCET dosage: unknown. During the same period patient was treated with AUGMENTIN, RABEPRAZOLE, ZOLOFT, AVLOCARDYL, VITAMINS B1 AND B6. Patient was hospitalized. Patient recovered.
Clozaril Side Effects Report #5284927-7
CLOZARIL problem was reported by a Physician from UNITED STATES on Apr 14, 2006. Female patient, 52 years of age, was diagnosed with schizoaffective disorder and was treated with CLOZARIL. After drug was administered, patient experienced the following problems/side effects: deep vein thrombosis, eosinophil count decreased, haematocrit decreased, haemoglobin decreased, influenza, leukopenia, lower respiratory tract infection, lymphocyte count decreased, lymphocyte percentage decreased, . CLOZARIL dosage: 75 MG, QHS, ORAL 50 MG, QD. During the same period patient was treated with PREVACID, ABILIFY, VERAPAMIL, METHADONE, LACTULOSE, LASIX, NOVOLIN NPH. Patient was hospitalized. Patient recovered.
Effexor Side Effects Report #5688487-8
Physician from FRANCE reported EFFEXOR problem on Mar 25, 2008. Male patient, weighting 143.3 lb, was diagnosed with depression, mesothelioma and was treated with EFFEXOR. After drug was administered, patient experienced the following problems/side effects: anti-platelet antibody positive, blood fibrinogen increased, eosinophil count decreased, fibrin d dimer increased, haemoglobin decreased, haptoglobin increased, lymphocyte count decreased, thrombocytopenia, . EFFEXOR dosage: unknown. During the same period patient was treated with FOLIC ACID, CYANOCOBALAMIN, CISPLATIN, ALIMTA. Patient was hospitalized. Patient recovered.
Zidovudine Side Effects Report #5493223-4
ZIDOVUDINE problem was reported by a Physician from SOUTH AFRICA on Oct 17, 2007. Male patient, weighting 7.72 lb, was treated with ZIDOVUDINE. After drug was administered, patient experienced the following problems/side effects: blood sodium decreased, cellulitis gangrenous, eosinophil count decreased, gastroenteritis, haematocrit decreased, haemoglobin decreased, lymphocyte count decreased, monocyte count decreased, neutropenia, . ZIDOVUDINE dosage: 12MG TWICE PER DAY. During the same period patient was treated with LAMIVUDINE, NELFINAVIR, AMPICILLIN, GENTAMICIN, CLOXACILLIN, PANADOL, ACYCLOVIR. Patient died on 04/08/2007.
Paxil Side Effects Report #5761168-8
Physician from JAPAN reported PAXIL problem on June 03, 2008. Male patient, 42 years of age, was diagnosed with depression and was treated with PAXIL. After drug was administered, patient experienced the following problems/side effects: alanine aminotransferase increased, aspartate aminotransferase increased, eosinophil count decreased, gamma-glutamyltransferase increased, liver disorder, nausea, neutrophil count decreased, ocular icterus, . PAXIL dosage: 20MG PER DAY. During the same period patient was treated with CARBAMAZEPINE, TRYPTANOL, SULPIRIDE, ETISEDAN, SEPAZON, MEILAX, NEUOMIL. Patient was hospitalized. Patient recovered.
Paxil Side Effects Report #5773904-5
PAXIL problem was reported by a Physician from JAPAN on June 13, 2008. Male patient, 42 years of age, was diagnosed with depression, trigeminal neuralgia, pain, tension headache and was treated with PAXIL. After drug was administered, patient experienced the following problems/side effects: alanine aminotransferase increased, aspartate aminotransferase increased, eosinophil count decreased, gamma-glutamyltransferase increased, liver disorder, liver function test abnormal, nausea, neutrophil count increased, ocular icterus, . PAXIL dosage: 20MG PER DAY. During the same period patient was treated with CARBAMAZEPINE, TRYPTANOL, SULPIRIDE, ETISEDAN, SEPAZON, MEILAX, NEUOMIL. Patient was hospitalized. Patient recovered.
Augmentin Side Effects Report #5753889-8
Consumer or non-health professional from FRANCE reported AUGMENTIN problem on May 21, 2008. Male patient, 62 years of age, was diagnosed with erysipelas, prostatitis and was treated with AUGMENTIN. After drug was administered, patient experienced the following problems/side effects: agranulocytosis, eosinophil count decreased, haemoglobin decreased, leukopenia, neutrophil percentage decreased, platelet count decreased, . AUGMENTIN dosage: unknown. During the same period patient was treated with OFLOCET, PARIET, ZOLOFT, AVLOCARDYL, VIT B. Patient was hospitalized. Patient died on 03/23/2008.