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PROTHROMBIN LEVEL DECREASED side effect

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Lovaza Side Effects Report #5691316-X
Consumer or non-health professional from UNITED STATES reported LOVAZA problem on Mar 21, 2008. Male patient was treated with LOVAZA. After drug was administered, patient experienced the following problems/side effects: prothrombin level decreased, . LOVAZA dosage: unknown. During the same period patient was treated with WARFARIN. Patient recovered.

Taxotere Side Effects Report #5541588-7
TAXOTERE problem was reported by a Physician from FRANCE on Dec 04, 2007. Male patient, 50 years of age, was treated with TAXOTERE. After drug was administered, patient experienced the following problems/side effects: prothrombin level decreased, . TAXOTERE dosage: unknown. During the same period patient was treated with FLUOROURACIL, ZYLORIC, NEUPOGEN, CISPLATIN. Patient was hospitalized. Patient recovered.

Risperdal Side Effects Report #5377024-3
Physician from FRANCE reported RISPERDAL problem on June 22, 2007. Male patient, 15 years of age, was diagnosed with psychotic disorder and was treated with RISPERDAL. After drug was administered, patient experienced the following problems/side effects: prothrombin level decreased, transaminases increased, weight increased, . RISPERDAL dosage: unknown. During the same period patient was treated with LOXAPAC, NEULEPTIL. Patient recovered.

Risperdal Side Effects Report #5377024-3
RISPERDAL problem was reported by a Physician from FRANCE on June 22, 2007. Male patient, 15 years of age, was diagnosed with psychotic disorder and was treated with RISPERDAL. After drug was administered, patient experienced the following problems/side effects: prothrombin level decreased, transaminases increased, weight increased, . RISPERDAL dosage: unknown. During the same period patient was treated with LOXAPAC, NEULEPTIL. Patient recovered.


Diprivan Side Effects Report #5352854-2
Health Professional from FRANCE reported DIPRIVAN problem on June 05, 2007. Male patient, 70 years of age, was treated with DIPRIVAN. After drug was administered, patient experienced the following problems/side effects: prothrombin level decreased, transaminases increased, . DIPRIVAN dosage: unknown. During the same period patient was treated with TRACRIUM, FENTANYL CITRATE, PERFALGAN, CEFAZOLIN, SEVORANE, AMLOR, LIPANTHYL. Patient was hospitalized. Patient recovered.

Celebrex Side Effects Report #5463439-1
CELEBREX problem was reported by a Physician from FRANCE on Sept 12, 2007. Female patient, 81 years of age, was diagnosed with back pain and was treated with CELEBREX. After drug was administered, patient experienced the following problems/side effects: back pain, prothrombin level decreased, red blood cell sedimentation rate abnormal, . CELEBREX dosage: DAILY DOSE:200MG. During the same period patient was treated with PREVISCAN, ANTIHYPERTENSIVES. Patient was hospitalized. Patient recovered.

Januvia Side Effects Report #5469472-8
Consumer or non-health professional from UNITED STATES reported JANUVIA problem on Apr 27, 2007. Female patient, 65 years of age, was treated with JANUVIA. After drug was administered, patient experienced the following problems/side effects: contusion, prothrombin level decreased, . JANUVIA dosage: 100 MG/DAILY/PO. During the same period patient was treated with COUMADIN, PLAVIX. Patient recovered.

Famciclovir Side Effects Report #5738620-4
FAMCICLOVIR problem was reported by a Consumer or non-health professional from AUSTRALIA on May 07, 2008. Female patient, 76 years of age, was diagnosed with herpes zoster and was treated with FAMCICLOVIR. After drug was administered, patient experienced the following problems/side effects: international normalised ratio increased, prothrombin level decreased, . FAMCICLOVIR dosage: 750 MG, QD. During the same period patient was treated with WARFARIN, CALCITRIOL, DIGOXIN, ENALAPRIL MALEATE, METHYLDOPA, VERAPAMIL HYDROCHLORIDE. Patient recovered.

Arixtra Side Effects Report #5360484-1
Health Professional from FRANCE reported ARIXTRA problem on June 08, 2007. Female patient, 76 years of age, weighting 110.2 lb, was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: ischaemic stroke, prothrombin level decreased, thrombocytopenia, thrombosis, visual disturbance, . ARIXTRA dosage: 5MG PER DAY. During the same period patient was treated with CORGARD, ISKEDYLT, ADANCOR, HYPERIUM, DISCOTRINE, OGAST, ASPIRIN. Patient died on 09/05/2006.


Arixtra Side Effects Report #5329995-9
ARIXTRA problem was reported by a Health Professional from FRANCE on May 10, 2007. Female patient, 76 years of age, was diagnosed with deep vein thrombosis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: ischaemic stroke, prothrombin level decreased, thrombocytopenia, thrombosis, visual disturbance, . ARIXTRA dosage: 5MG PER DAY. Patient died on 09/05/2006.

Vfend Side Effects Report #5665007-5
Physician from JAPAN reported VFEND problem on Mar 03, 2008. Female patient, 27 years of age, was treated with VFEND. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, gamma-glutamyltransferase increased, prothrombin level decreased, pyrexia, . VFEND dosage: DAILY DOSE:400MG. Patient recovered.

Flagyl Side Effects Report #5511131-7
FLAGYL problem was reported by a Consumer or non-health professional from on Nov 01, 2007. Female patient, 58 years of age, was diagnosed with inflammation and was treated with FLAGYL. After drug was administered, patient experienced the following problems/side effects: hepatocellular damage, international normalised ratio increased, prothrombin level decreased, transaminases increased, . FLAGYL dosage: unknown. During the same period patient was treated with CALCIUM, VITAMIN E, PREDNISOLONE. Patient was hospitalized. Patient recovered.

Lodoz Side Effects Report #5500304-5
Consumer or non-health professional from FRANCE reported LODOZ problem on Oct 10, 2007. Female patient, 57 years of age, was diagnosed with crohn's disease and was treated with LODOZ. After drug was administered, patient experienced the following problems/side effects: leukopenia, neutropenia, prothrombin level decreased, prothrombin time ratio decreased, tachycardia, thrombocytopenia, urosepsis, . LODOZ dosage: unknown. During the same period patient was treated with REMICADE, RABEPRAZOLE, ATARAX, ZOLPIDEM TARTRATE, LOVENOX, AUGMENTIN. Patient was hospitalized. Patient recovered.

Augmentin Side Effects Report #5451432-4
AUGMENTIN problem was reported by a Consumer or non-health professional from FRANCE on Sept 03, 2007. Female patient, 86 years of age, was treated with AUGMENTIN. After drug was administered, patient experienced the following problems/side effects: international normalised ratio increased, prothrombin level decreased, . AUGMENTIN dosage: unknown. During the same period patient was treated with PREVISCAN, COVERSYL, DIAMICRON, POTASSIUM CHLORIDE, ACARBOSE, ACETAMINOPHEN, LASIX. Patient was hospitalized. Patient recovered.


Celebrex Side Effects Report #5471943-5
Physician from FRANCE reported CELEBREX problem on Sept 21, 2007. Female patient, 81 years of age, was diagnosed with back pain and was treated with CELEBREX. After drug was administered, patient experienced the following problems/side effects: back pain, dehydration, prothrombin level decreased, red blood cell sedimentation rate abnormal, urinary tract infection, . CELEBREX dosage: DAILY DOSE:200MG. During the same period patient was treated with PREVISCAN, ANTIHYPERTENSIVES. Patient was hospitalized. Patient recovered.

Amlodipine Side Effects Report #5379371-8
AMLODIPINE problem was reported by a Health Professional from SPAIN on June 13, 2007. Female patient, 46 years of age, was diagnosed with essential hypertension and was treated with AMLODIPINE. After drug was administered, patient experienced the following problems/side effects: encephalopathy, hepatitis, prothrombin level decreased, . AMLODIPINE dosage: unknown. During the same period patient was treated with ATENOLOL, TELMISARTAN, HYDROCHLOROTHIAZIDE. Patient was hospitalized. Patient recovered.

Amlodipine Side Effects Report #5381132-0
Health Professional from SPAIN reported AMLODIPINE problem on June 27, 2007. Female patient, 46 years of age, was diagnosed with essential hypertension and was treated with AMLODIPINE. After drug was administered, patient experienced the following problems/side effects: hepatic encephalopathy, hepatitis, prothrombin level decreased, . AMLODIPINE dosage: unknown. During the same period patient was treated with ATENOLOL, TELMISARTAN, HYDROCHLOROTHIAZIDE. Patient was hospitalized. Patient recovered.

Zeclar Side Effects Report #5386087-0
ZECLAR problem was reported by a Physician from FRANCE on July 04, 2007. Female patient, 63 years of age, was diagnosed with helicobacter infection and was treated with ZECLAR. After drug was administered, patient experienced the following problems/side effects: haemorrhage, prothrombin level decreased, . ZECLAR dosage: unknown. During the same period patient was treated with ANTIVITAMIN K ANTICOAGULANT. Patient recovered.

Zithromax Side Effects Report #5386772-0
Health Professional from FRANCE reported ZITHROMAX problem on July 03, 2007. Male patient, weighting 112.4 lb, was treated with ZITHROMAX. After drug was administered, patient experienced the following problems/side effects: anaemia, joint effusion, prothrombin level decreased, . ZITHROMAX dosage: unknown. During the same period patient was treated with PREVISCAN, KARDEGIC, INIPOMP, LASIX, NITRODERM. Patient was hospitalized. Patient recovered.


Amlodipine Side Effects Report #5379371-8
AMLODIPINE problem was reported by a Health Professional from SPAIN on June 13, 2007. Female patient, 46 years of age, was diagnosed with essential hypertension and was treated with AMLODIPINE. After drug was administered, patient experienced the following problems/side effects: encephalopathy, hepatitis, prothrombin level decreased, . AMLODIPINE dosage: unknown. During the same period patient was treated with ATENOLOL, TELMISARTAN, HYDROCHLOROTHIAZIDE. Patient was hospitalized. Patient recovered.

Amlodipine Side Effects Report #5381132-0
Health Professional from SPAIN reported AMLODIPINE problem on June 27, 2007. Female patient, 46 years of age, was diagnosed with essential hypertension and was treated with AMLODIPINE. After drug was administered, patient experienced the following problems/side effects: hepatic encephalopathy, hepatitis, prothrombin level decreased, . AMLODIPINE dosage: unknown. During the same period patient was treated with ATENOLOL, TELMISARTAN, HYDROCHLOROTHIAZIDE. Patient was hospitalized. Patient recovered.

Zeclar Side Effects Report #5386087-0
ZECLAR problem was reported by a Physician from FRANCE on July 04, 2007. Female patient, 63 years of age, was diagnosed with helicobacter infection and was treated with ZECLAR. After drug was administered, patient experienced the following problems/side effects: haemorrhage, prothrombin level decreased, . ZECLAR dosage: unknown. During the same period patient was treated with ANTIVITAMIN K ANTICOAGULANT. Patient recovered.

Zithromax Side Effects Report #5386772-0
Health Professional from FRANCE reported ZITHROMAX problem on July 03, 2007. Male patient, weighting 112.4 lb, was treated with ZITHROMAX. After drug was administered, patient experienced the following problems/side effects: anaemia, joint effusion, prothrombin level decreased, . ZITHROMAX dosage: unknown. During the same period patient was treated with PREVISCAN, KARDEGIC, INIPOMP, LASIX, NITRODERM. Patient was hospitalized. Patient recovered.

Escitalopram Side Effects Report #5782109-3
ESCITALOPRAM problem was reported by a Health Professional from FRANCE on June 04, 2008. Female patient, 77 years of age, was diagnosed with breast cancer, post procedural complication and was treated with ESCITALOPRAM. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, prothrombin level decreased, subcutaneous haematoma, . ESCITALOPRAM dosage: unknown. During the same period patient was treated with ARIXTRA, KARDEGIC, PROPYLTHIOURACILE, INEXIUM, ALPRAZOLAM. Patient was hospitalized. Patient recovered.

Klacid Side Effects Report #5699550-X
Health Professional from SWEDEN reported KLACID problem on Apr 01, 2008. Female patient, 67 years of age, was diagnosed with pneumonia, atrial fibrillation and was treated with KLACID. After drug was administered, patient experienced the following problems/side effects: intra-abdominal haemorrhage, prothrombin level decreased, . KLACID dosage: unknown. During the same period patient was treated with WARFARIN, TIOTROPIUM BROMIDE, SIMVASTATIN, OMEPRAZOLE, NITROLINGUAL SUBLINGUAL, PARACETAMOL, DIAZEPAM, DIGOXIN. Patient was hospitalized. Patient recovered.

Vfend Side Effects Report #5717086-4
VFEND problem was reported by a Physician from JAPAN on Apr 16, 2008. Female patient, 27 years of age, was treated with VFEND. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, gamma-glutamyltransferase increased, prothrombin level decreased, pyrexia, . VFEND dosage: DAILY DOSE:400MG. Patient recovered.

Micardis Side Effects Report #5349863-6
Physician from reported MICARDIS HCT problem on June 07, 2007. Female patient, 46 years of age, was diagnosed with essential hypertension and was treated with MICARDIS HCT. After drug was administered, patient experienced the following problems/side effects: hepatic encephalopathy, hepatitis fulminant, prothrombin level decreased, . MICARDIS HCT dosage: unknown. During the same period patient was treated with TENORMIN, AMLODIPINO, ENALAPRIL MALEATE. Patient recovered.

Tenormin Side Effects Report #5360797-3
TENORMIN problem was reported by a Health Professional from SPAIN on June 13, 2007. Female patient, 46 years of age, was diagnosed with essential hypertension and was treated with TENORMIN. After drug was administered, patient experienced the following problems/side effects: encephalopathy, hepatitis, prothrombin level decreased, . TENORMIN dosage: unknown. During the same period patient was treated with MICARDIS HCT, AMLODIPINO. Patient was hospitalized. Patient recovered.

Cymbalta Side Effects Report #5367850-9
Physician from UNITED STATES reported CYMBALTA problem on June 15, 2007. Female patient, 85 years of age, was diagnosed with depression and was treated with CYMBALTA. After drug was administered, patient experienced the following problems/side effects: international normalised ratio decreased, prothrombin level decreased, . CYMBALTA dosage: 60 MG, UNK. During the same period patient was treated with COUMADIN, EFFEXOR. Patient recovered.

Cymbalta Side Effects Report #5368830-X
CYMBALTA problem was reported by a Physician from UNITED STATES on June 15, 2007. Female patient, 85 years of age, was diagnosed with depression and was treated with CYMBALTA. After drug was administered, patient experienced the following problems/side effects: international normalised ratio decreased, prothrombin level decreased, . CYMBALTA dosage: 60 MG, UNK. During the same period patient was treated with COUMADIN, EFFEXOR. Patient recovered.

Sevorane Side Effects Report #5374026-8
Health Professional from FRANCE reported SEVORANE LIQUID INHALATION problem on June 21, 2007. Male patient, 70 years of age, was treated with SEVORANE LIQUID INHALATION. After drug was administered, patient experienced the following problems/side effects: alanine aminotransferase increased, cytolytic hepatitis, prothrombin level decreased, . SEVORANE LIQUID INHALATION dosage: unknown. During the same period patient was treated with PARACETAMOL, ATRACURIUM BESYLATE, PROPOFOL, FENTANYL, CEFAZOLIN, AMLODIPINE, FENOFIBRATE, TAMSULOSINE. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5316889-8
ARIXTRA problem was reported by a Physician from FRANCE on Apr 24, 2007. Female patient, 84 years of age, was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: international normalised ratio increased, off label use, prothrombin level decreased, renal failure, retroperitoneal haematoma, retroperitoneal haemorrhage, . ARIXTRA dosage: 7.5MG PER DAY. Patient was hospitalized. Patient recovered.

Tahor Side Effects Report #5284021-5
Health Professional from FRANCE reported TAHOR problem on Mar 21, 2007. Female patient, 75 years of age, was treated with TAHOR. After drug was administered, patient experienced the following problems/side effects: anaemia, prothrombin level decreased, . TAHOR dosage: unknown. During the same period patient was treated with OMEPRAZOLE, TRAMADOL, PREVISCAN, INDAPAMIDE, METOPROLOL TARTRATE, PRETERAX. Patient was hospitalized. Patient recovered.

Zithromax Side Effects Report #5292498-4
ZITHROMAX problem was reported by a Health Professional from FRANCE on Mar 29, 2007. Male patient, weighting 112.4 lb, was treated with ZITHROMAX. After drug was administered, patient experienced the following problems/side effects: anaemia, joint effusion, prothrombin level decreased, . ZITHROMAX dosage: unknown. During the same period patient was treated with PREVISCAN, KARDEGIC, INIPOMP, LASIX, NITRODERM. Patient was hospitalized. Patient recovered.

Lysodren Side Effects Report #5296068-3
Pharmacist from FRANCE reported LYSODREN problem on Mar 02, 2007. Male patient, 53 years of age, was diagnosed with adrenocortical carcinoma, adrenal insufficiency, asthma, hypertension and was treated with LYSODREN. After drug was administered, patient experienced the following problems/side effects: cholestasis, prothrombin level decreased, . LYSODREN dosage: unknown. During the same period patient was treated with HYDROCORTISONE, SERETIDE, ATACAND. Patient died on 02/08/2007.

Depakene Side Effects Report #5282013-3
DEPAKENE problem was reported by a Health Professional from FRANCE on Mar 23, 2007. Male patient, 79 years of age, was diagnosed with convulsion and was treated with DEPAKENE. After drug was administered, patient experienced the following problems/side effects: blood fibrinogen increased, coagulation factor vii level decreased, prothrombin level decreased, prothrombin time shortened, thrombocytopenia, . DEPAKENE dosage: unknown. Patient was hospitalized. Patient recovered.