HAEMORRHAGE SUBCUTANEOUS side effect
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Drugs associated with HAEMORRHAGE SUBCUTANEOUS
ADDERALL AMOXICILLIN ARIXTRA AROMASIN ASPIRIN AVONEX BETAFERON CELECOX CELECOXIB CHANTIX CIPROFLOXACIN CLARITHROMYCIN CYMBALTA DOXIL FLIXOTIDE FLOVENT FOSAMAX FRAGMIN HALCION KLARICID LAMISIL LANSOPRAZOLE LEXAPRO LIPIDIL LIPITOR LUVOX METAMIZOLE MEVALOTIN MICONAZOLE NORVASC PAXIL PLAVIX POLLAKISU PRAVASTATIN RABEPRAZOLE RELPAX REQUIP RISEDRONATE RISPERDAL SERETIDE SORAFENIB SULFAMETHOXAZOLE SULPERAZON TICLOPIDINE VFEND VIAGRA ZANTAC ZETIA ZITHROMAX ZOLADEX ZYPREXAAromasin Side Effects Report #5649743-2
Physician from JAPAN reported AROMASIN problem on Feb 21, 2008. Female patient, 51 years of age, was treated with AROMASIN. After drug was administered, patient experienced the following problems/side effects: haemorrhage subcutaneous, . AROMASIN dosage: unknown. During the same period patient was treated with XELODA. Patient recovered.
Risperdal Side Effects Report #5664595-2
RISPERDAL problem was reported by a Pharmacist from JAPAN on Mar 05, 2008. Female patient, 33 years of age, was treated with RISPERDAL. After drug was administered, patient experienced the following problems/side effects: haemorrhage subcutaneous, . RISPERDAL dosage: unknown. Patient recovered.
Lexapro Side Effects Report #5616213-7
Pharmacist from DENMARK reported LEXAPRO problem on Jan 21, 2008. Female patient, 42 years of age, was diagnosed with depression and was treated with LEXAPRO. After drug was administered, patient experienced the following problems/side effects: haemorrhage subcutaneous, overdose, . LEXAPRO dosage: 25 MG QD PO. During the same period patient was treated with ESKIM. Patient recovered.
Aspirin Side Effects Report #5588303-9
ASPIRIN problem was reported by a Pharmacist from JAPAN on Jan 08, 2008. Female patient, 78 years of age, was treated with ASPIRIN. After drug was administered, patient experienced the following problems/side effects: haemorrhage subcutaneous, pancytopenia, . ASPIRIN dosage: TOTAL DAILY DOSE: 100 MG UNIT DOSE: 100 MG. During the same period patient was treated with OMEPRAL. Patient was hospitalized. Patient recovered.
Zoladex Side Effects Report #5593340-4
Physician from JAPAN reported ZOLADEX problem on Jan 09, 2008. Male patient, 85 years of age, was diagnosed with prostate cancer and was treated with ZOLADEX. After drug was administered, patient experienced the following problems/side effects: haemorrhage subcutaneous, . ZOLADEX dosage: unknown. Patient was hospitalized. Patient recovered.
Requip Side Effects Report #5600114-4
REQUIP problem was reported by a Health Professional from NETHERLANDS on Jan 15, 2008. Female patient, 57 years of age, was diagnosed with parkinson's disease and was treated with REQUIP. After drug was administered, patient experienced the following problems/side effects: haemorrhage subcutaneous, rash macular, retinal haemorrhage, urticaria, . REQUIP dosage: 2MG THREE TIMES PER DAY. During the same period patient was treated with AZILECT. Patient recovered.
Amoxicillin Side Effects Report #5602525-X
Physician from JAPAN reported AMOXICILLIN TRIHYDRATE problem on Jan 21, 2008. Male patient, 40 years of age, was treated with AMOXICILLIN TRIHYDRATE. After drug was administered, patient experienced the following problems/side effects: haemorrhage subcutaneous, hepatic enzyme increased, myalgia, . AMOXICILLIN TRIHYDRATE dosage: 750MG THREE TIMES PER DAY. Patient recovered.
Viagra Side Effects Report #5535343-1
VIAGRA problem was reported by a Consumer or non-health professional from JAPAN on Nov 26, 2007. Male patient, 69 years of age, was treated with VIAGRA. After drug was administered, patient experienced the following problems/side effects: haemorrhage subcutaneous, penile haemorrhage, . VIAGRA dosage: DAILY DOSE:12.5MG. Patient recovered.
Lexapro Side Effects Report #5557362-1
Consumer or non-health professional from IRELAND reported LEXAPRO problem on Nov 26, 2007. Female patient, 42 years of age, was diagnosed with depression and was treated with LEXAPRO. After drug was administered, patient experienced the following problems/side effects: haemorrhage subcutaneous, overdose, . LEXAPRO dosage: 25 MG QD PO. During the same period patient was treated with ESKIM. Patient recovered.
Arixtra Side Effects Report #5557610-8
ARIXTRA problem was reported by a Physician from FRANCE on Dec 06, 2007. Female patient, 85 years of age, weighting 110.2 lb, was diagnosed with bedridden, parkinson's disease and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: haemorrhage subcutaneous, muscle haemorrhage, skin ulcer, . ARIXTRA dosage: 2.5MG PER DAY. During the same period patient was treated with LASIX, HEMIGOXINE, MODOPAR. Patient recovered.
Zithromax Side Effects Report #5508203-X
Physician from JAPAN reported ZITHROMAX problem on Oct 25, 2007. Female patient, 17 years of age, was diagnosed with empyema and was treated with ZITHROMAX. After drug was administered, patient experienced the following problems/side effects: haemorrhage subcutaneous, platelet count decreased, . ZITHROMAX dosage: unknown. During the same period patient was treated with EXPECTORANTS. Patient recovered.
Sulperazon Side Effects Report #5479028-9
SULPERAZON problem was reported by a Physician from CHINA on Sept 25, 2007. Female patient, 64 years of age, was diagnosed with lung infection and was treated with SULPERAZON. After drug was administered, patient experienced the following problems/side effects: haemorrhage subcutaneous, injection site haemorrhage, subcutaneous haematoma, . SULPERAZON dosage: unknown. Patient recovered.
Rabeprazole Side Effects Report #5485948-1
Physician from SAUDI ARABIA reported RABEPRAZOLE problem on Oct 01, 2007. Male patient was diagnosed with helicobacter infection and was treated with RABEPRAZOLE. After drug was administered, patient experienced the following problems/side effects: haemorrhage subcutaneous, international normalised ratio increased, . RABEPRAZOLE dosage: 20 MG, 1 IN 1 D, ORAL; 40 MG, 2 IN 1 D, ORAL. During the same period patient was treated with WARFARIN, CLARITHROMYCIN, AMOXICILLIN. Patient recovered.
Pollakisu Side Effects Report #5502749-6
POLLAKISU problem was reported by a Pharmacist from JAPAN on Oct 19, 2007. Female patient, 78 years of age, was treated with POLLAKISU. After drug was administered, patient experienced the following problems/side effects: haemorrhage subcutaneous, . POLLAKISU dosage: unknown. During the same period patient was treated with ANTICOAGULANT. Patient recovered.
Sulperazon Side Effects Report #5503312-3
Physician from CHINA reported SULPERAZON problem on Oct 19, 2007. Female patient, 64 years of age, was diagnosed with lung infection and was treated with SULPERAZON. After drug was administered, patient experienced the following problems/side effects: haemorrhage subcutaneous, injection site haemorrhage, subcutaneous haematoma, . SULPERAZON dosage: unknown. Patient recovered.
Paxil Side Effects Report #5450137-3
PAXIL problem was reported by a Pharmacist from JAPAN on Sept 10, 2007. Male patient, 47 years of age, was diagnosed with depression, hernia, insomnia and was treated with PAXIL. After drug was administered, patient experienced the following problems/side effects: haemorrhage subcutaneous, . PAXIL dosage: 10MG THREE TIMES PER DAY. During the same period patient was treated with LORCAM, METHYCOBAL, SILECE, CYTOTEC, NEUROTROPIN, VOLTAREN. Patient recovered.
Arixtra Side Effects Report #5450140-3
Physician from JAPAN reported ARIXTRA problem on Sept 10, 2007. Female patient, 67 years of age, weighting 116.8 lb, was diagnosed with thrombosis prophylaxis, osteoporosis, conjunctivitis, insomnia, pain and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: haemorrhage subcutaneous, post procedural haematoma, post procedural swelling, wound complication, . ARIXTRA dosage: 2.5MG PER DAY. During the same period patient was treated with RISEDRONATE, HYPEN, MUCOSTA, FERROMIA, TARIVID, RHYTHMY, INDOMETHACIN, HARTMANNS. Patient was hospitalized. Patient recovered.
Celecoxib Side Effects Report #5403275-5
CELECOXIB problem was reported by a Physician from JAPAN on July 24, 2007. Female patient, 75 years of age, was diagnosed with back pain and was treated with CELECOXIB. After drug was administered, patient experienced the following problems/side effects: haemorrhage subcutaneous, prothrombin time prolonged, . CELECOXIB dosage: unknown. During the same period patient was treated with WARFARIN. Patient was hospitalized. Patient recovered.
Paxil Side Effects Report #5416733-4
Pharmacist from JAPAN reported PAXIL problem on Aug 09, 2007. Female patient, 86 years of age, was diagnosed with depression and was treated with PAXIL. After drug was administered, patient experienced the following problems/side effects: haemorrhage subcutaneous, . PAXIL dosage: 10MG PER DAY. During the same period patient was treated with PREDONINE, TANNALBIN, LAC B, FUROSEMIDE. Patient was hospitalized. Patient recovered.
Paxil Side Effects Report #5380784-9
PAXIL problem was reported by a Pharmacist from JAPAN on July 03, 2007. Male patient, 47 years of age, was diagnosed with depression, hernia, insomnia and was treated with PAXIL. After drug was administered, patient experienced the following problems/side effects: haemorrhage subcutaneous, . PAXIL dosage: 10MG THREE TIMES PER DAY. During the same period patient was treated with LORCAM, CYANOCOBALAMIN, SILECE, CYTOTEC, NEUROTROPIN, VOLTAREN. Patient recovered.
Paxil Side Effects Report #5380784-9
Pharmacist from JAPAN reported PAXIL problem on July 03, 2007. Male patient, 47 years of age, was diagnosed with depression, hernia, insomnia and was treated with PAXIL. After drug was administered, patient experienced the following problems/side effects: haemorrhage subcutaneous, . PAXIL dosage: 10MG THREE TIMES PER DAY. During the same period patient was treated with LORCAM, CYANOCOBALAMIN, SILECE, CYTOTEC, NEUROTROPIN, VOLTAREN. Patient recovered.
Aromasin Side Effects Report #5765855-7
AROMASIN problem was reported by a Physician from JAPAN on May 30, 2008. Female patient, weighting 112.4 lb, was diagnosed with breast cancer and was treated with AROMASIN. After drug was administered, patient experienced the following problems/side effects: haemorrhage subcutaneous, . AROMASIN dosage: unknown. Patient recovered.
Luvox Side Effects Report #5768141-4
Consumer or non-health professional from GERMANY reported LUVOX problem on May 21, 2008. Female patient, 38 years of age, was diagnosed with social phobia and was treated with LUVOX. After drug was administered, patient experienced the following problems/side effects: haemorrhage subcutaneous, . LUVOX dosage: unknown. During the same period patient was treated with LORAZEPAM, SULPIRIDE, CLONAZEPAM. Patient recovered.
Zetia Side Effects Report #5774621-8
ZETIA problem was reported by a Physician from JAPAN on June 06, 2008. Male patient, 56 years of age, was diagnosed with hyperlipidaemia and was treated with ZETIA. After drug was administered, patient experienced the following problems/side effects: haemorrhage subcutaneous, pancytopenia, . ZETIA dosage: unknown. During the same period patient was treated with PIOGLITAZONE HYDROCHLORIDE. Patient was hospitalized. Patient recovered.
Doxil Side Effects Report #5775084-9
Physician from JAPAN reported DOXIL problem on June 06, 2008. Female patient, 61 years of age, was diagnosed with ovarian cancer and was treated with DOXIL. After drug was administered, patient experienced the following problems/side effects: haemorrhage subcutaneous, herpes dermatitis, stomatitis, . DOXIL dosage: unknown. Patient recovered.
Luvox Side Effects Report #5783032-0
LUVOX problem was reported by a Consumer or non-health professional from GERMANY on June 04, 2008. Female patient, 38 years of age, was diagnosed with social phobia and was treated with LUVOX. After drug was administered, patient experienced the following problems/side effects: haemorrhage subcutaneous, . LUVOX dosage: 25 MG, 1 D), ORAL, (50 MG, 1 D), ORAL, (100 MG, 1 D), ORAL , (150 MG, 1 D), ORAL. During the same period patient was treated with LORAZEPAM, SULPIRIDE, CLONAZEPAM. Patient recovered.
Arixtra Side Effects Report #5747814-3
Physician from JAPAN reported ARIXTRA problem on May 21, 2008. Female patient, 84 years of age, was diagnosed with thrombosis prophylaxis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: haemorrhage subcutaneous, joint swelling, . ARIXTRA dosage: 1.5MG PER DAY. Patient recovered.
Arixtra Side Effects Report #5700319-8
ARIXTRA problem was reported by a Physician from JAPAN on Apr 04, 2008. Female patient, 74 years of age, was diagnosed with thrombosis prophylaxis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: haemorrhage subcutaneous, oedema peripheral, thrombosis, . ARIXTRA dosage: 1.5MG PER DAY. Patient was hospitalized. Patient recovered.
Relpax Side Effects Report #5342778-9
Physician from JAPAN reported RELPAX problem on May 22, 2007. Female patient, 25 years of age, was diagnosed with migraine and was treated with RELPAX. After drug was administered, patient experienced the following problems/side effects: haemorrhage subcutaneous, . RELPAX dosage: DAILY DOSE:40MG. Patient recovered.
Paxil Side Effects Report #5372211-2
PAXIL problem was reported by a Pharmacist from JAPAN on June 26, 2007. Male patient, 47 years of age, was diagnosed with depression and was treated with PAXIL. After drug was administered, patient experienced the following problems/side effects: haemorrhage subcutaneous, . PAXIL dosage: 10MG THREE TIMES PER DAY. During the same period patient was treated with LORCAM, CYANOCOBALAMIN, SILECE, CYTOTEC, NEUROTROPIN. Patient recovered.
Risedronate Side Effects Report #5318501-0
Physician from JAPAN reported RISEDRONATE problem on Apr 20, 2007. Male patient, 82 years of age, was diagnosed with osteoporosis and was treated with RISEDRONATE. After drug was administered, patient experienced the following problems/side effects: haemorrhage subcutaneous, purpura, thrombocytopenia, . RISEDRONATE dosage: 2.5 MG DAILY, ORAL. During the same period patient was treated with NORVASC, ANTIHYPERTENSIVES. Patient was hospitalized. Patient recovered.
Zyprexa Side Effects Report #5337989-2
ZYPREXA problem was reported by a Physician from JAPAN on May 16, 2007. Male patient, 19 years of age, was diagnosed with schizophrenia, constipation and was treated with ZYPREXA. After drug was administered, patient experienced the following problems/side effects: haemorrhage subcutaneous, . ZYPREXA dosage: 7.5 MG, DAILY (1/D). During the same period patient was treated with PURSENNID. Patient recovered.
Fosamax Side Effects Report #5285419-1
Health Professional from UNITED KINGDOM reported FOSAMAX problem on Mar 30, 2007. Male patient, 74 years of age, weighting 147.7 lb, was diagnosed with osteoporosis, hypertension, benign prostatic hyperplasia and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: haemorrhage subcutaneous, . FOSAMAX dosage: unknown. During the same period patient was treated with ASPIRIN, BENDROFLUMETHIAZIDE, CALCIUM CARBONATE, FINASTERIDE, TAMSULOSIN HYDROCHLORIDE. Patient recovered.
Zyprexa Side Effects Report #5289694-9
ZYPREXA problem was reported by a Physician from JAPAN on Mar 23, 2007. Male patient, 19 years of age, was diagnosed with schizophrenia, constipation and was treated with ZYPREXA. After drug was administered, patient experienced the following problems/side effects: haemorrhage subcutaneous, . ZYPREXA dosage: 7.5 MG, DAILY (1/D). During the same period patient was treated with PURSENNID. Patient recovered.
Halcion Side Effects Report #5310746-9
Pharmacist from JAPAN reported HALCION problem on Apr 17, 2007. Female patient was treated with HALCION. After drug was administered, patient experienced the following problems/side effects: haemorrhage subcutaneous, purpura, . HALCION dosage: DAILY DOSE:.25MG. During the same period patient was treated with CONTOMIN, BIPERIDEN HYDROCHLORIDE, SEPAZON, LENDORMIN. Patient recovered.
Vfend Side Effects Report #5253630-1
VFEND problem was reported by a Physician from JAPAN on Feb 19, 2007. Female patient, 85 years of age, was diagnosed with bronchopulmonary aspergillosis, pneumonia and was treated with VFEND. After drug was administered, patient experienced the following problems/side effects: haemorrhage subcutaneous, platelet count decreased, . VFEND dosage: DAILY DOSE:400MG. During the same period patient was treated with TIENAM. Patient recovered.
Vfend Side Effects Report #5256690-7
Physician from JAPAN reported VFEND problem on Feb 26, 2007. Female patient was diagnosed with bronchopulmonary aspergillosis, pneumonia and was treated with VFEND. After drug was administered, patient experienced the following problems/side effects: haemorrhage subcutaneous, interstitial lung disease, platelet count decreased, . VFEND dosage: DAILY DOSE:400MG. During the same period patient was treated with TIENAM, PREDONINE, PRIDOL, OMEPRAL, HALOPERIDOL, VITAMEDIN CAPSULE. Patient died on 02/22/2007.
Flixotide Side Effects Report #5267318-4
FLIXOTIDE problem was reported by a Consumer or non-health professional from NETHERLANDS on Mar 06, 2007. Female patient was treated with FLIXOTIDE. After drug was administered, patient experienced the following problems/side effects: haemorrhage subcutaneous, skin atrophy, . FLIXOTIDE dosage: unknown. During the same period patient was treated with ACENOCOUMAROL, EUCARDIC, SPIRONOLACTONE, PROMOCARD. Patient recovered.
Vfend Side Effects Report #5276297-5
Physician from JAPAN reported VFEND problem on Mar 14, 2007. Female patient was diagnosed with bronchopulmonary aspergillosis, pneumonia and was treated with VFEND. After drug was administered, patient experienced the following problems/side effects: haemorrhage subcutaneous, interstitial lung disease, platelet count decreased, . VFEND dosage: DAILY DOSE:240MG-FREQ:DAILY. During the same period patient was treated with TIENAM, PREDONINE, PRIDOL, OMEPRAL, HALOPERIDOL, VITAMEDIN CAPSULE. Patient died on 02/22/2007.
Arixtra Side Effects Report #5646976-6
ARIXTRA problem was reported by a Physician from JAPAN on Feb 26, 2008. Male patient, 56 years of age, weighting 169.8 lb, was diagnosed with thrombosis prophylaxis, hypertension, gout, analgesia, rheumatoid arthritis, diabetes mellitus and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: cardiovascular disorder, haemorrhage subcutaneous, post procedural haemorrhage, swelling, wound dehiscence, wound haemorrhage, wound secretion, . ARIXTRA dosage: 2.5MG PER DAY. During the same period patient was treated with DIOVAN, URINORM, VOLTAREN, GASTER D, CELESTAMINE, RIMATIL, CRESTOR, AMARYL. Patient was hospitalized. Patient recovered.
Arixtra Side Effects Report #5661256-0
Physician from JAPAN reported ARIXTRA problem on Mar 07, 2008. Male patient, 59 years of age, weighting 130.1 lb, was diagnosed with thrombosis prophylaxis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, haemorrhage subcutaneous, pain, platelet count increased, red blood cell count decreased, white blood cell count increased, . ARIXTRA dosage: 2.5MG PER DAY. During the same period patient was treated with RHEUMATREX, AZULFIDINE EN, PROGRAF, PREDONINE, HEPARIN. Patient was hospitalized and became disabled. Patient recovered.
Arixtra Side Effects Report #5682850-7
ARIXTRA problem was reported by a Physician from JAPAN on Mar 25, 2008. Male patient, 59 years of age, weighting 130.1 lb, was diagnosed with thrombosis prophylaxis, rheumatoid arthritis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, haemorrhage subcutaneous, pain, platelet count increased, red blood cell count decreased, white blood cell count increased, . ARIXTRA dosage: 2.5MG PER DAY. During the same period patient was treated with RHEUMATREX, AZULFIDINE EN, PROGRAF, PREDONINE, HEPARIN. Patient was hospitalized and became disabled. Patient recovered.
Zantac Side Effects Report #5620263-4
Physician from JAPAN reported ZANTAC problem on Feb 05, 2008. Female patient, 55 years of age, was diagnosed with deafness neurosensory and was treated with ZANTAC. After drug was administered, patient experienced the following problems/side effects: haematoma, haemorrhage subcutaneous, platelet count decreased, thrombocytopenic purpura, . ZANTAC dosage: 150MG TWICE PER DAY. During the same period patient was treated with PREDNISOLONE, CYANOCOBALAMIN, ADETPHOS, ISOSORBID. Patient recovered.
Arixtra Side Effects Report #5624688-2
ARIXTRA problem was reported by a Pharmacist from JAPAN on Feb 07, 2008. Female patient, 70 years of age, weighting 143.3 lb, was diagnosed with thrombosis prophylaxis, infection prophylaxis, analgesia, insomnia and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: delirium, haemorrhage subcutaneous, injection site bruising, insomnia, restlessness, speech disorder, . ARIXTRA dosage: 2.5MG PER DAY. During the same period patient was treated with CEFAMEZIN, SEISHOKU, PENTAZOCINE LACTATE, MYSLEE, LENDORMIN. Patient recovered.
Zantac Side Effects Report #5645335-X
Physician from JAPAN reported ZANTAC problem on Feb 25, 2008. Female patient, 55 years of age, was diagnosed with deafness neurosensory and was treated with ZANTAC. After drug was administered, patient experienced the following problems/side effects: haematoma, haemorrhage subcutaneous, platelet count decreased, thrombocytopenic purpura, white blood cell count increased, . ZANTAC dosage: 150MG TWICE PER DAY. During the same period patient was treated with PREDNISOLONE, CYANOCOBALAMIN, ADETPHOS, ISOSORBID. Patient recovered.
Mevalotin Side Effects Report #5598582-X
MEVALOTIN problem was reported by a Pharmacist from JAPAN on Jan 11, 2008. Female patient, 87 years of age, was diagnosed with cerebrovascular disorder and was treated with MEVALOTIN. After drug was administered, patient experienced the following problems/side effects: electrocardiogram qt prolonged, haemorrhage subcutaneous, pancytopenia, . MEVALOTIN dosage: 10 MG. During the same period patient was treated with ALLOPURINOL, MEDITRANS, TAKEPRON OD, LASIX, PLAVIX. Patient recovered.
Plavix Side Effects Report #5621118-1
Consumer or non-health professional from UNITED STATES reported PLAVIX problem on Jan 15, 2007. Female patient was treated with PLAVIX. After drug was administered, patient experienced the following problems/side effects: eye haemorrhage, haemorrhage subcutaneous, . PLAVIX dosage: unknown. Patient recovered.
Klaricid Side Effects Report #5565740-X
KLARICID problem was reported by a Consumer or non-health professional from JAPAN on Dec 10, 2007. Female patient, weighting 102.5 lb, was diagnosed with upper respiratory tract inflammation, diabetes mellitus, angina pectoris, upper respiratory tract infection and was treated with KLARICID. After drug was administered, patient experienced the following problems/side effects: haemorrhage subcutaneous, hypoglycaemia, . KLARICID dosage: unknown. During the same period patient was treated with GLICLAZIDE, WARFARIN POTASSIUM, WARFARIN POTASSIUM, WARFARIN POTASSIUM, BUCOLOME, PRANLUKAST HYDRATE. Patient was hospitalized. Patient recovered.
Klaricid Side Effects Report #5573889-0
Consumer or non-health professional from JAPAN reported KLARICID problem on Dec 20, 2007. Female patient, weighting 102.5 lb, was diagnosed with upper respiratory tract inflammation, diabetes mellitus, angina pectoris, upper respiratory tract infection and was treated with KLARICID. After drug was administered, patient experienced the following problems/side effects: haemorrhage subcutaneous, hypoglycaemia, . KLARICID dosage: unknown. During the same period patient was treated with GLICLAZIDE, WARFARIN POTASSIUM, WARFARIN POTASSIUM, WARFARIN POTASSIUM, BUCOLOME, PRANLUKAST HYDRATE. Patient was hospitalized. Patient recovered.
Arixtra Side Effects Report #5574959-3
ARIXTRA problem was reported by a Pharmacist from JAPAN on Dec 21, 2007. Female patient, 70 years of age, weighting 143.3 lb, was diagnosed with thrombosis prophylaxis, infection prophylaxis, analgesia, insomnia and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: delirium, haemorrhage subcutaneous, injection site bruising, insomnia, restlessness, speech disorder, . ARIXTRA dosage: 2.5MG PER DAY. During the same period patient was treated with CEFAMEZIN, SEISHOKU, PENTAZOCINE LACTATE, MYSLEE, LENDORMIN. Patient recovered.
Pravastatin Side Effects Report #5511600-X
Pharmacist from JAPAN reported PRAVASTATIN problem on Nov 02, 2007. Female patient, 87 years of age, was diagnosed with cerebrovascular disorder and was treated with PRAVASTATIN. After drug was administered, patient experienced the following problems/side effects: electrocardiogram qt prolonged, haemorrhage subcutaneous, pancytopenia, . PRAVASTATIN dosage: 10 MG. During the same period patient was treated with ALLOPURINOL, MEDITRANS, TAKEPRON OD, LASIX, PLAVIX. Patient recovered.