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COAGULATION TIME PROLONGED side effect

What is COAGULATION TIME PROLONGED ?
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Drugs associated with COAGULATION TIME PROLONGED

ANGIOMAX  ARAVA  ARGATROBAN  ASPIRIN  AUGMENTIN  CHAMPIX  COMTAN  COREG  COUMADIN  DIPRIVAN  ELIDEL  FEVERALL  FORTEO  GABAPENTIN  HEPARIN  IBUPROFEN  INTEGRILIN  ITRACONAZOLE  LEVAQUIN  NATALIZUMAB  NEXIUM  NIFEDIPINE  NOLVADEX  PLAVIX  PREVISCAN  REVLIMID  STROMECTOL  TARCEVA  TIPRANAVIR  ULTIVA  VALPROATE  VARENICLINE  VELCADE  VESICARE  VINCRISTINE  WARFARIN  ZESTORETIC  ZOCOR  


Arava Side Effects Report #5660699-9
Pharmacist from UNITED STATES reported ARAVA problem on Mar 04, 2008. Female patient, 64 years of age, was treated with ARAVA. After drug was administered, patient experienced the following problems/side effects: coagulation time prolonged, faeces discoloured, haemorrhage, . ARAVA dosage: unknown. During the same period patient was treated with WARFARIN, METHOTREXATE, PREDNISONE, LIPITOR. Patient was hospitalized. Patient recovered.

Augmentin Side Effects Report #5632109-9
AUGMENTIN problem was reported by a Consumer or non-health professional from GREECE on Feb 12, 2008. Female patient, child 5 years of age, was diagnosed with lower respiratory tract infection and was treated with AUGMENTIN. After drug was administered, patient experienced the following problems/side effects: coagulation time prolonged, hyperbilirubinaemia, jaundice, ocular icterus, transaminases increased, . AUGMENTIN dosage: 8ML THREE TIMES PER DAY. During the same period patient was treated with AEROLIN, FLIXOTIDE. Patient was hospitalized. Patient recovered.

Gabapentin Side Effects Report #5632636-4
Health Professional from UNITED KINGDOM reported GABAPENTIN problem on Feb 08, 2008. Female patient, 74 years of age, was diagnosed with neuralgia and was treated with GABAPENTIN. After drug was administered, patient experienced the following problems/side effects: coagulation time prolonged, international normalised ratio increased, subdural haematoma, . GABAPENTIN dosage: unknown. During the same period patient was treated with DIGOXIN, ENALAPRIL MALEATE, FERROUS SULPHATE, WARFARIN. Patient recovered.

Gabapentin Side Effects Report #5635693-4
GABAPENTIN problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Feb 07, 2008. Female patient, 74 years of age, was diagnosed with neuralgia and was treated with GABAPENTIN. After drug was administered, patient experienced the following problems/side effects: coagulation time prolonged, international normalised ratio increased, subdural haematoma, . GABAPENTIN dosage: 300 MG, TID, ORAL. During the same period patient was treated with WARFARIN, FERROUS SULPHATE. Patient recovered.


Warfarin Side Effects Report #5643384-9
Consumer or non-health professional from CANADA reported WARFARIN problem on Feb 11, 2008. Male patient, 77 years of age, was diagnosed with cardiac disorder and was treated with WARFARIN. After drug was administered, patient experienced the following problems/side effects: coagulation time prolonged, conjunctival haemorrhage, dyspnoea, fatigue, haemoglobin decreased, international normalised ratio increased, post procedural complication, . WARFARIN dosage: unknown. Patient recovered.

Angiomax Side Effects Report #5648152-X
ANGIOMAX problem was reported by a Physician from UNITED STATES on Feb 19, 2008. Male patient was diagnosed with percutaneous coronary intervention and was treated with ANGIOMAX. After drug was administered, patient experienced the following problems/side effects: coagulation time prolonged, coronary artery dissection, coronary artery thrombosis, procedural complication, . ANGIOMAX dosage: 0.75 MG/KG, BOLUS, INTRAVENOUS; 1.75 MG/KG, HR, INTRAEVNOUS. During the same period patient was treated with ASPIRIN. Patient recovered.

Heparin Side Effects Report #5602051-8
Pharmacist from UNITED STATES reported HEPARIN problem on Jan 22, 2008. Male patient, 73 years of age, weighting 198.4 lb, was diagnosed with carotid endarterectomy and was treated with HEPARIN. After drug was administered, patient experienced the following problems/side effects: coagulation time prolonged, nonspecific reaction, therapeutic response decreased, . HEPARIN dosage: unknown. Patient recovered.

Plavix Side Effects Report #5622554-X
PLAVIX problem was reported by a Health Professional from UNITED STATES on Oct 23, 2007. Male patient, 63 years of age, weighting 180.8 lb, was diagnosed with coronary artery bypass, mitral valve replacement and was treated with PLAVIX. After drug was administered, patient experienced the following problems/side effects: coagulation time prolonged, post procedural haemorrhage, . PLAVIX dosage: unknown. During the same period patient was treated with ANGIOMAX. Patient recovered.

Revlimid Side Effects Report #5646881-5
Pharmacist from UNITED STATES reported REVLIMID problem on Nov 08, 2007. Female patient, 54 years of age, was diagnosed with multiple myeloma and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: coagulation time prolonged, dizziness, fall, . REVLIMID dosage: 10, 5 MG, QD X 21 DAYS, ORAL. During the same period patient was treated with WARFARIN. Patient was hospitalized. Patient recovered.


Comtan Side Effects Report #5564547-7
COMTAN problem was reported by a Health Professional from BRAZIL on Dec 10, 2007. Female patient, weighting 110.2 lb, was diagnosed with parkinson's disease and was treated with COMTAN. After drug was administered, patient experienced the following problems/side effects: coagulation time prolonged, epistaxis, haematoma, international normalised ratio increased, prothrombin time prolonged, . COMTAN dosage: unknown. During the same period patient was treated with MAREVAN. Patient recovered.

Angiomax Side Effects Report #5573521-6
Pharmacist from UNITED STATES reported ANGIOMAX problem on Dec 20, 2007. Female patient, 65 years of age, weighting 191.8 lb, was diagnosed with percutaneous coronary intervention and was treated with ANGIOMAX. After drug was administered, patient experienced the following problems/side effects: coagulation time prolonged, . ANGIOMAX dosage: 65MG ONCE IV BOLUS; 152MG/HR DRIP IV DRIP. Patient recovered.

Angiomax Side Effects Report #5506541-8
ANGIOMAX problem was reported by a Pharmacist from UNITED STATES on Oct 19, 2007. Male patient, 71 years of age, weighting 179.0 lb, was diagnosed with percutaneous coronary intervention and was treated with ANGIOMAX. After drug was administered, patient experienced the following problems/side effects: coagulation time prolonged, overdose, . ANGIOMAX dosage: 0.75 MG/KG, BOLUS, IV BOLUS; 0.75 MG/KG, HR, INTRAVENOUS. During the same period patient was treated with PLAVIX, COUMADIN. Patient recovered.

Itraconazole Side Effects Report #5521044-2
Physician from UNITED STATES reported ITRACONAZOLE problem on Nov 08, 2007. Female patient, 54 years of age, weighting 171.1 lb, was diagnosed with fungal infection, heparin-induced thrombocytopenia and was treated with ITRACONAZOLE. After drug was administered, patient experienced the following problems/side effects: coagulation time prolonged, hepatic enzyme increased, . ITRACONAZOLE dosage: unknown. During the same period patient was treated with ARGATROBAN, ALBUTEROL, DOCUSATE, SENNA, INSULIN, CALCIUM CARBONATE, PREDNISONE, METOCLOPRAMIDE. Patient was hospitalized. Patient recovered.

Natalizumab Side Effects Report #5533580-3
NATALIZUMAB problem was reported by a Health Professional from UNITED STATES on Nov 20, 2007. Female patient, 49 years of age, weighting 126.0 lb, was diagnosed with multiple sclerosis and was treated with NATALIZUMAB. After drug was administered, patient experienced the following problems/side effects: coagulation time prolonged, condition aggravated, haematotoxicity, international normalised ratio increased, multiple sclerosis, nosocomial infection, sepsis, staphylococcal infection, . NATALIZUMAB dosage: 300 MG;QM;IV. Patient was hospitalized. Patient recovered.


Levaquin Side Effects Report #5492204-4
Consumer or non-health professional from UNITED STATES reported LEVAQUIN problem on Oct 15, 2007. Male patient, 87 years of age, weighting 190.0 lb, was diagnosed with sinus polyp, atrial fibrillation, renal impairment, blood cholesterol increased, hypertension and was treated with LEVAQUIN. After drug was administered, patient experienced the following problems/side effects: coagulation time prolonged, diarrhoea, muscular weakness, skin discolouration, . LEVAQUIN dosage: unknown. During the same period patient was treated with WARFARIN, CALCITRIOL, COZAAR, ALLOPURINOL, ISOSORBIDE DINITRATE, ZOCOR, PREDNISONE. Patient recovered.

Warfarin Side Effects Report #5503840-0
WARFARIN problem was reported by a Physician from UNITED STATES on Oct 15, 2007. Male patient, 81 years of age, was treated with WARFARIN. After drug was administered, patient experienced the following problems/side effects: coagulation time prolonged, ecchymosis, international normalised ratio increased, . WARFARIN dosage: unknown. During the same period patient was treated with DOXYCYCLINE HYCLATE, LOTEPREDNOL ETABONATE, NIASPAN, ATENOLOL, ZESTRIL, IMDUR, PREVACID, PROSCAR. Patient recovered.

Vesicare Side Effects Report #5486606-X
Consumer or non-health professional from UNITED STATES reported VESICARE problem on June 07, 2007. Female patient, 70 years of age, was diagnosed with hypertonic bladder and was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: coagulation time prolonged, constipation, dry mouth, rotator cuff syndrome, vision blurred, . VESICARE dosage: 10 MG, UID/QD. During the same period patient was treated with COUMADIN, OMEPRAZOLE, ALEVE, LOPRESSOR, ACCUPRIL, INSULIN, LEVOTHYROXINE, ASPIRIN. Patient recovered.

Nexium Side Effects Report #5409830-0
NEXIUM problem was reported by a Health Professional from SWITZERLAND on Aug 02, 2007. Female patient, 97 years of age, weighting 180.8 lb, was diagnosed with atrial fibrillation, atrial flutter and was treated with NEXIUM. After drug was administered, patient experienced the following problems/side effects: coagulation time prolonged, . NEXIUM dosage: unknown. During the same period patient was treated with SINTROM, MORPHINE SULPHATE, PRACTO, PASPERTIN. Patient recovered.

Levaquin Side Effects Report #5429521-X
Consumer or non-health professional from UNITED STATES reported LEVAQUIN problem on Aug 22, 2007. Male patient, 87 years of age, weighting 190.0 lb, was diagnosed with sinus polyp, atrial fibrillation, renal impairment, blood cholesterol increased, hypertension and was treated with LEVAQUIN. After drug was administered, patient experienced the following problems/side effects: coagulation time prolonged, diarrhoea, muscular weakness, skin discolouration, . LEVAQUIN dosage: unknown. During the same period patient was treated with WARFARIN, CALCITRIOL, COZAAR, ALLOPURINOL, ISOSORBIDE DINITRATE, ZOCOR. Patient recovered.


Previscan Side Effects Report #5378779-4
PREVISCAN problem was reported by a Health Professional from FRANCE on June 22, 2007. Female patient, 57 years of age, was diagnosed with mitral valve disease, depression, intentional overdose and was treated with PREVISCAN. After drug was administered, patient experienced the following problems/side effects: coagulation time prolonged, intentional overdose, loss of consciousness, . PREVISCAN dosage: unknown. During the same period patient was treated with EFFEXOR, CORDARONE, MEPRONIZINE, TRANXENE, ZOLPIDEM TARTRATE. Patient was hospitalized. Patient recovered.

Previscan Side Effects Report #5378779-4
Health Professional from FRANCE reported PREVISCAN problem on June 22, 2007. Female patient, 57 years of age, was diagnosed with mitral valve disease, depression, intentional overdose and was treated with PREVISCAN. After drug was administered, patient experienced the following problems/side effects: coagulation time prolonged, intentional overdose, loss of consciousness, . PREVISCAN dosage: unknown. During the same period patient was treated with EFFEXOR, CORDARONE, MEPRONIZINE, TRANXENE, ZOLPIDEM TARTRATE. Patient was hospitalized. Patient recovered.

Argatroban Side Effects Report #5802554-7
ARGATROBAN problem was reported by a Physician from UNITED STATES on Oct 08, 2007. Female patient, 71 years of age, was diagnosed with heparin-induced thrombocytopenia and was treated with ARGATROBAN. After drug was administered, patient experienced the following problems/side effects: coagulation time prolonged, . ARGATROBAN dosage: unknown. Patient was hospitalized. Patient recovered.

Heparin Side Effects Report #5728939-5
Pharmacist from UNITED STATES reported HEPARIN ECTION problem on Apr 28, 2008. Female patient was treated with HEPARIN ECTION. After drug was administered, patient experienced the following problems/side effects: coagulation time prolonged, . HEPARIN ECTION dosage: unknown. During the same period patient was treated with HEPARIN ECTION. Patient recovered.

Warfarin Side Effects Report #5739563-2
WARFARIN problem was reported by a Consumer or non-health professional from UNITED STATES on May 09, 2008. Female patient, weighting 154.3 lb, was diagnosed with cerebrovascular accident prophylaxis, thrombosis prophylaxis, constipation and was treated with WARFARIN. After drug was administered, patient experienced the following problems/side effects: coagulation time prolonged, constipation, . WARFARIN dosage: unknown. During the same period patient was treated with DULCOLAX. Patient was hospitalized. Patient recovered.

Heparin Side Effects Report #5746381-8
Health Professional from UNITED STATES reported HEPARIN ECTION problem on May 15, 2008. Female patient, 68 years of age, weighting 240.3 lb, was diagnosed with extracorporeal circulation and was treated with HEPARIN ECTION. After drug was administered, patient experienced the following problems/side effects: coagulation time prolonged, . HEPARIN ECTION dosage: unknown. During the same period patient was treated with HEPARIN ECTION. Patient recovered.

Gabapentin Side Effects Report #5692807-8
GABAPENTIN problem was reported by a Health Professional from UNITED KINGDOM on Feb 07, 2008. Female patient was diagnosed with neuralgia, atrial fibrillation and was treated with GABAPENTIN. After drug was administered, patient experienced the following problems/side effects: coagulation time prolonged, subdural haematoma, . GABAPENTIN dosage: 300 MG; TID; PO. During the same period patient was treated with DIGOXIN, WARFARIN, ENALAPRIL MALEATE, FERROUS SULPHATE. Patient recovered.

Augmentin Side Effects Report #5700919-5
Consumer or non-health professional from GREECE reported AUGMENTIN problem on Apr 03, 2008. Female patient, child 5 years of age, was diagnosed with lower respiratory tract infection and was treated with AUGMENTIN. After drug was administered, patient experienced the following problems/side effects: coagulation time prolonged, hyperbilirubinaemia, jaundice, ocular icterus, transaminases increased, . AUGMENTIN dosage: 8ML THREE TIMES PER DAY. During the same period patient was treated with AEROLIN, FLUTICASONE PROPIONATE. Patient was hospitalized. Patient recovered.

Heparin Side Effects Report #5716006-6
HEPARIN ECTION problem was reported by a Pharmacist from UNITED STATES on Jan 29, 2008. Female patient, 78 years of age, weighting 145.0 lb, was treated with HEPARIN ECTION. After drug was administered, patient experienced the following problems/side effects: coagulation time prolonged, haemorrhage, . HEPARIN ECTION dosage: unknown. During the same period patient was treated with HEPARIN ECTION. Patient recovered.

Argatroban Side Effects Report #5345137-8
Pharmacist from UNITED STATES reported ARGATROBAN problem on May 21, 2007. Female patient, 70 years of age, weighting 101.0 lb, was diagnosed with coagulopathy and was treated with ARGATROBAN. After drug was administered, patient experienced the following problems/side effects: coagulation time prolonged, international normalised ratio increased, . ARGATROBAN dosage: unknown. During the same period patient was treated with DIGOXIN, ERYTHROPOIETIN, PHENYTOIN, INSULIN, LABETALOL, PREVACID, VERSED. Patient died on 05/18/2007.

Argatroban Side Effects Report #5354628-5
ARGATROBAN problem was reported by a Health Professional from GERMANY on May 25, 2007. Male patient, 61 years of age, was diagnosed with heparin-induced thrombocytopenia and was treated with ARGATROBAN. After drug was administered, patient experienced the following problems/side effects: coagulation time prolonged, . ARGATROBAN dosage: unknown. During the same period patient was treated with HEPARIN. Patient died.

Comtan Side Effects Report #5360187-3
Health Professional from BRAZIL reported COMTAN problem on June 06, 2007. Female patient, weighting 110.2 lb, was diagnosed with parkinson's disease and was treated with COMTAN. After drug was administered, patient experienced the following problems/side effects: coagulation time prolonged, epistaxis, haematoma, international normalised ratio increased, prothrombin time prolonged, . COMTAN dosage: unknown. During the same period patient was treated with MAREVAN. Patient recovered.

Argatroban Side Effects Report #5370068-7
ARGATROBAN problem was reported by a Pharmacist from UNITED STATES on Oct 13, 2006. Male patient, 70 years of age, weighting 211.6 lb, was diagnosed with heparin-induced thrombocytopenia, pre-existing disease and was treated with ARGATROBAN. After drug was administered, patient experienced the following problems/side effects: coagulation time prolonged, . ARGATROBAN dosage: unknown. During the same period patient was treated with ASCORBIC ACID, REGULAR INSULIN, NOVOLOG, PREDNISONE, PROCRIT, COREG. Patient was hospitalized. Patient recovered.

Argatroban Side Effects Report #5370070-5
Pharmacist from UNITED STATES reported ARGATROBAN problem on Aug 09, 2006. Female patient, 78 years of age, was diagnosed with heparin-induced thrombocytopenia and was treated with ARGATROBAN. After drug was administered, patient experienced the following problems/side effects: coagulation time prolonged, . ARGATROBAN dosage: unknown. During the same period patient was treated with DIGOXIN, FAMOTIDINE, METOPROLOL SUCCINATE. Patient was hospitalized. Patient recovered.

Vesicare Side Effects Report #5372975-8
VESICARE problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 05, 2007. Female patient, 70 years of age, was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: coagulation time prolonged, constipation, dry mouth, vision blurred, . VESICARE dosage: 10 MG. During the same period patient was treated with COUMADIN. Patient recovered.

Stromectol Side Effects Report #5314829-9
Physician from JAPAN reported STROMECTOL problem on Apr 24, 2007. Female patient, 70 years of age, weighting 77.16 lb, was diagnosed with acarodermatitis, prophylaxis, hypertension, arrhythmia, nausea, hyperlipidaemia, gastritis and was treated with STROMECTOL. After drug was administered, patient experienced the following problems/side effects: coagulation time prolonged, gastroenteritis, prescribed overdose, . STROMECTOL dosage: unknown. During the same period patient was treated with WARFARIN, AMLODIN, RYTHMODAN, LANIRAPID, GASMOTIN, MEVALOTIN, ZANTAC. Patient was hospitalized. Patient recovered.

Stromectol Side Effects Report #5321898-9
STROMECTOL problem was reported by a Physician from JAPAN on May 02, 2007. Female patient, 70 years of age, weighting 77.16 lb, was diagnosed with acarodermatitis, prophylaxis, hypertension, arrhythmia, nausea, hyperlipidaemia, gastritis and was treated with STROMECTOL. After drug was administered, patient experienced the following problems/side effects: coagulation time prolonged, gastrointestinal disorder, prescribed overdose, . STROMECTOL dosage: unknown. During the same period patient was treated with WARFARIN, AMLODIN, RYTHMODAN, LANIRAPID, GASMOTIN, MEVALOTIN, ZANTAC. Patient was hospitalized. Patient recovered.

Vincristine Side Effects Report #5325784-X
Consumer or non-health professional from SWITZERLAND reported VINCRISTINE problem on Sept 19, 2005. Female patient, 83 years of age, was diagnosed with b-cell lymphoma, thyroid disorder, urinary tract infection and was treated with VINCRISTINE. After drug was administered, patient experienced the following problems/side effects: coagulation time prolonged, disease recurrence, hepatitis b, hepatitis chronic active, hepatitis infectious, hepatitis toxic, urinary tract infection, . VINCRISTINE dosage: 1.8 MG, 1 IN 3 WK), INTRAVENOUS (NOT OTHERWISE SPECIFIED). During the same period patient was treated with DOXORUBICIN HYDROCHLORIDE, PANTOPRAZOLE, CARBIMAZOLE, RITUXIMAB, CYCLOPHOSPHAMIDE, CIPROFLOXACIN, CALCIUM CARBONATE, TORSEMIDE. Patient was hospitalized. Patient recovered.

Stromectol Side Effects Report #5328804-1
STROMECTOL problem was reported by a Physician from JAPAN on May 14, 2007. Female patient, 70 years of age, weighting 77.16 lb, was diagnosed with acarodermatitis, prophylaxis, hypertension, arrhythmia, nausea, hyperlipidaemia, gastritis and was treated with STROMECTOL. After drug was administered, patient experienced the following problems/side effects: coagulation time prolonged, gastrointestinal disorder, prescribed overdose, . STROMECTOL dosage: unknown. During the same period patient was treated with WARFARIN, AMLODIN, RYTHMODAN, LANIRAPID, GASMOTIN, MEVALOTIN, ZANTAC. Patient recovered.

Ibuprofen Side Effects Report #5295903-2
Health Professional from UNITED KINGDOM reported IBUPROFEN problem on Apr 04, 2007. Male patient, 38 years of age, was treated with IBUPROFEN. After drug was administered, patient experienced the following problems/side effects: coagulation time prolonged, liver disorder, overdose, sepsis, . IBUPROFEN dosage: unknown. During the same period patient was treated with ACETAMINOPHEN. Patient was hospitalized. Patient died.

Ibuprofen Side Effects Report #5299716-7
IBUPROFEN problem was reported by a Consumer or non-health professional from DENMARK on Mar 29, 2007. Male patient, 52 years of age, was diagnosed with podagra and was treated with IBUPROFEN. After drug was administered, patient experienced the following problems/side effects: coagulation time prolonged, international normalised ratio increased, . IBUPROFEN dosage: unknown. During the same period patient was treated with WARFARIN, TIAPROFENIC ACID, ALLOPURINOL, ERGOCALCIFEROL, FUROSEMIDE, NIFEDIPINE, CETIRIZINE, CALCIUM CARBONATE. Patient was hospitalized. Patient recovered.

Ibuprofen Side Effects Report #5306416-3
Physician from DENMARK reported IBUPROFEN problem on Apr 10, 2007. Male patient, 52 years of age, weighting 143.3 lb, was diagnosed with arthritis, thrombosis prophylaxis and was treated with IBUPROFEN. After drug was administered, patient experienced the following problems/side effects: coagulation time prolonged, international normalised ratio increased, . IBUPROFEN dosage: unknown. During the same period patient was treated with MAREVANTE, SURGAMYL. Patient was hospitalized. Patient recovered.

Champix Side Effects Report #5312874-0
CHAMPIX problem was reported by a Pharmacist from FRANCE on Apr 18, 2007. Female patient, weighting 105.8 lb, was treated with CHAMPIX. After drug was administered, patient experienced the following problems/side effects: coagulation time prolonged, ecchymosis, haematoma, international normalised ratio increased, prothrombin time prolonged, . CHAMPIX dosage: unknown. During the same period patient was treated with COUMADIN, ANTITHROMBOTIC AGENTS. Patient recovered.

Nolvadex Side Effects Report #5265181-9
Consumer or non-health professional from UNITED STATES reported NOLVADEX problem on Dec 07, 2004. Female patient, 77 years of age, weighting 127.0 lb, was diagnosed with breast cancer and was treated with NOLVADEX. After drug was administered, patient experienced the following problems/side effects: coagulation time prolonged, thrombosis, . NOLVADEX dosage: 20 MG QD PO. During the same period patient was treated with WARFARIN, FOSAMAX. Patient was hospitalized. Patient recovered.

Tipranavir Side Effects Report #5273160-0
TIPRANAVIR problem was reported by a Consumer or non-health professional from UNITED STATES MINOR OUTLYING ISLANDS on Mar 19, 2007. Female patient, weighting 49.01 lb, was diagnosed with hiv infection, retroviral infection, medical diet, antifungal prophylaxis, antibiotic prophylaxis, increased appetite and was treated with TIPRANAVIR. After drug was administered, patient experienced the following problems/side effects: coagulation time prolonged, contusion, . TIPRANAVIR dosage: TPV/RTV 510 MG/202 MG. During the same period patient was treated with ABACAVIR, SIDERAL, FOLIC ACID, BACTRIM, ZITHROMAX, PERIACTIN. Patient recovered.

Diprivan Side Effects Report #5280626-6
Health Professional from FRANCE reported DIPRIVAN problem on Mar 26, 2007. Female patient, child 2 years of age, was diagnosed with anaesthesia and was treated with DIPRIVAN. After drug was administered, patient experienced the following problems/side effects: coagulation time prolonged, . DIPRIVAN dosage: unknown. During the same period patient was treated with HYPNOVEL, SEVOFLURANE, MINISINTROM, DESFLURANE, PERFALGAN, KETAMINE. Patient recovered.

Champix Side Effects Report #5282231-4
CHAMPIX problem was reported by a Pharmacist from FRANCE on Mar 19, 2007. Female patient, 38 years of age, was treated with CHAMPIX. After drug was administered, patient experienced the following problems/side effects: coagulation time prolonged, haematoma, . CHAMPIX dosage: unknown. During the same period patient was treated with COUMADIN. Patient recovered.

Heparin Side Effects Report #5636317-2
Physician from UNITED STATES reported HEPARIN problem on Feb 25, 2008. Male patient, 71 years of age, weighting 169.8 lb, was diagnosed with catheterisation cardiac and was treated with HEPARIN. After drug was administered, patient experienced the following problems/side effects: cerebrovascular accident, coagulation time prolonged, thrombosis, . HEPARIN dosage: unknown. Patient was hospitalized and became disabled. Patient recovered.

Heparin Side Effects Report #5602028-2
HEPARIN problem was reported by a Pharmacist from UNITED STATES on Jan 22, 2008. Male patient, 77 years of age, weighting 224.9 lb, was diagnosed with coronary artery bypass and was treated with HEPARIN. After drug was administered, patient experienced the following problems/side effects: blood pressure decreased, coagulation time prolonged, . HEPARIN dosage: unknown. Patient recovered.

Argatroban Side Effects Report #5574142-1
Health Professional from UNITED STATES reported ARGATROBAN problem on Dec 11, 2007. Female patient, 49 years of age, was diagnosed with thrombosis prophylaxis and was treated with ARGATROBAN. After drug was administered, patient experienced the following problems/side effects: activated partial thromboplastin time prolonged, coagulation time prolonged, haemoglobin decreased, hypotension, international normalised ratio increased, thrombocytopenia, thrombosis in device, . ARGATROBAN dosage: 40 MG, INTRAVENOUS; 10 MG, INTRAVENOUS; 22 MG, INTRAVENOUS. During the same period patient was treated with INSULIN, CALCIUM CHLORIDE, MAGNESIUM SULPHATE, NEO SYNEPHRINE. Patient recovered.

Elidel Side Effects Report #5505945-7
ELIDEL problem was reported by a Physician from BRAZIL on Oct 26, 2007. Male patient, 22 years of age, was diagnosed with dermatitis atopic and was treated with ELIDEL. After drug was administered, patient experienced the following problems/side effects: bleeding time prolonged, coagulation time prolonged, . ELIDEL dosage: unknown. Patient recovered.

Tarceva Side Effects Report #5531422-3
Health Professional from CANADA reported TARCEVA problem on Nov 13, 2007. Male patient, 59 years of age, was treated with TARCEVA. After drug was administered, patient experienced the following problems/side effects: asthenia, coagulation time prolonged, diarrhoea, mouth ulceration, muscle spasticity, rash vesicular, . TARCEVA dosage: 150 MG, QD, ORAL. During the same period patient was treated with BISOPROLOL FUMARATE, CITALOPRAM HYDROBROMIDE, LANSOPRAZOLE, AVELOX, THEOPHYLLINE, MIRTAZAPINE. Patient recovered.

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