ACTIVATED PARTIAL THROMBOPLASTIN TIME ABNORMAL side effect
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Drugs associated with ACTIVATED PARTIAL THROMBOPLASTIN TIME ABNORMAL
CEREZYME FLUOXETINE HEPARIN KALETRA KETOROLAC NEBILOXFluoxetine Side Effects Report #5554879-0
Physician from UNITED KINGDOM reported FLUOXETINE problem on Dec 04, 2007. Female patient, 41 years of age, weighting 189.6 lb, was diagnosed with depression, pain and was treated with FLUOXETINE. After drug was administered, patient experienced the following problems/side effects: activated partial thromboplastin time abnormal, . FLUOXETINE dosage: 20 MG, UNK. Patient recovered.
Fluoxetine Side Effects Report #5565669-7
FLUOXETINE problem was reported by a Health Professional from UNITED KINGDOM on Dec 04, 2007. Female patient was diagnosed with depression, pain and was treated with FLUOXETINE. After drug was administered, patient experienced the following problems/side effects: activated partial thromboplastin time abnormal, . FLUOXETINE dosage: 20 MG, UNK. Patient recovered.
Fluoxetine Side Effects Report #5566728-5
Health Professional from UNITED KINGDOM reported FLUOXETINE problem on Dec 04, 2007. Female patient, 41 years of age, was diagnosed with depression and was treated with FLUOXETINE. After drug was administered, patient experienced the following problems/side effects: activated partial thromboplastin time abnormal, . FLUOXETINE dosage: unknown. Patient recovered.
Fluoxetine Side Effects Report #5569974-X
FLUOXETINE problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Dec 04, 2007. Female patient, 41 years of age, weighting 189.6 lb, was diagnosed with depression and was treated with FLUOXETINE. After drug was administered, patient experienced the following problems/side effects: activated partial thromboplastin time abnormal, . FLUOXETINE dosage: 20 MG ORAL. During the same period patient was treated with CODEINE PHOSPHATE AND ACETAMINOPHEN. Patient recovered.
Fluoxetine Side Effects Report #5572332-5
Health Professional from UNITED KINGDOM reported FLUOXETINE problem on Dec 04, 2007. Female patient, 41 years of age, weighting 189.6 lb, was diagnosed with depression and was treated with FLUOXETINE. After drug was administered, patient experienced the following problems/side effects: activated partial thromboplastin time abnormal, . FLUOXETINE dosage: 20 MG; ; ORAL. Patient recovered.
Fluoxetine Side Effects Report #5572393-3
FLUOXETINE problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Dec 05, 2007. Female patient, 41 years of age, was diagnosed with depression and was treated with FLUOXETINE. After drug was administered, patient experienced the following problems/side effects: activated partial thromboplastin time abnormal, . FLUOXETINE dosage: 20 MG;QD;PO. Patient recovered.
Kaletra Side Effects Report #5470277-2
Consumer or non-health professional from ISRAEL reported KALETRA problem on Sept 17, 2007. Male patient, weighting 108.0 lb, was diagnosed with hiv infection and was treated with KALETRA. After drug was administered, patient experienced the following problems/side effects: activated partial thromboplastin time abnormal, blood fibrinogen abnormal, blood lactate dehydrogenase abnormal, burkitt's lymphoma, hepatic neoplasm malignant, hepatomegaly, pleural effusion, pneumonia bacterial, . KALETRA dosage: unknown. During the same period patient was treated with TENOFOVIR DISOPROXIL FUMARATE, LAMIVUDINE. Patient was hospitalized. Patient recovered.
Kaletra Side Effects Report #5397228-3
KALETRA problem was reported by a Consumer or non-health professional from ISRAEL on July 15, 2007. Male patient, weighting 108.0 lb, was diagnosed with hiv infection and was treated with KALETRA. After drug was administered, patient experienced the following problems/side effects: activated partial thromboplastin time abnormal, blood fibrinogen abnormal, blood lactate dehydrogenase abnormal, burkitt's lymphoma, hepatic neoplasm malignant, hepatomegaly, pleural effusion, pneumonia bacterial, . KALETRA dosage: unknown. During the same period patient was treated with TENOFOVIR, LAMIVUDINE. Patient was hospitalized. Patient recovered.
Kaletra Side Effects Report #5397228-3
Consumer or non-health professional from ISRAEL reported KALETRA problem on July 15, 2007. Male patient, weighting 108.0 lb, was diagnosed with hiv infection and was treated with KALETRA. After drug was administered, patient experienced the following problems/side effects: activated partial thromboplastin time abnormal, blood fibrinogen abnormal, blood lactate dehydrogenase abnormal, burkitt's lymphoma, hepatic neoplasm malignant, hepatomegaly, pleural effusion, pneumonia bacterial, . KALETRA dosage: unknown. During the same period patient was treated with TENOFOVIR, LAMIVUDINE. Patient was hospitalized. Patient recovered.
Nebilox Side Effects Report #5730358-2
NEBILOX problem was reported by a Physician from FRANCE on Apr 18, 2008. Female patient, 86 years of age, was treated with NEBILOX. After drug was administered, patient experienced the following problems/side effects: activated partial thromboplastin time abnormal, bradycardia, c-reactive protein increased, international normalised ratio increased, malaise, oedema, orthostatic hypotension, platelet count decreased, red blood cell count decreased, . NEBILOX dosage: unknown. During the same period patient was treated with LEVOTHYROXINE, NEO MERCAZOLE, XALATAN, PREVISCAN, STILNOX, TARDYFERON. Patient was hospitalized. Patient recovered.
Heparin Side Effects Report #5745300-8
Health Professional from UNITED STATES reported HEPARIN ECTION problem on May 09, 2008. Female patient was treated with HEPARIN ECTION. After drug was administered, patient experienced the following problems/side effects: activated partial thromboplastin time abnormal, incorrect dose administered, . HEPARIN ECTION dosage: unknown. Patient recovered.
Cerezyme Side Effects Report #5330475-5
CEREZYME problem was reported by a Physician from PORTUGAL on May 07, 2007. Male patient, 33 years of age, weighting 116.8 lb, was diagnosed with gaucher's disease and was treated with CEREZYME. After drug was administered, patient experienced the following problems/side effects: activated partial thromboplastin time abnormal, cerebral haematoma, cerebral haemorrhage, echocardiogram abnormal, hyperreflexia, laboratory test abnormal, platelet count increased, prothrombin time abnormal, . CEREZYME dosage: unknown. During the same period patient was treated with ALENDRONIC ACID. Patient was hospitalized. Patient recovered.
Ketorolac Side Effects Report #5684879-1
Pharmacist from UNITED STATES reported KETOROLAC TROMETHAMINE problem on Feb 09, 1996. Female patient, 13 years of age, weighting 90.39 lb, was diagnosed with back pain and was treated with KETOROLAC TROMETHAMINE. After drug was administered, patient experienced the following problems/side effects: abdominal pain, activated partial thromboplastin time abnormal, hepatic enzyme increased, intra-abdominal haemorrhage, leukopenia, prothrombin time abnormal, thrombocytopenia, vomiting, . KETOROLAC TROMETHAMINE dosage: unknown. During the same period patient was treated with ANTIBIOTIC NOS. Patient was hospitalized. Patient died on 05/20/1995.