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Acetylsalicylic Side Effects Report #5650820-0
Pharmacist from ITALY reported ACETYLSALICYLIC ACID SRT problem on Feb 29, 2008. Female patient, 83 years of age, was diagnosed with thrombosis prophylaxis and was treated with ACETYLSALICYLIC ACID SRT. After drug was administered, patient experienced the following problems/side effects: mouth haemorrhage, . ACETYLSALICYLIC ACID SRT dosage: TOTAL DAILY DOSE: 100 MG UNIT DOSE: 100 MG. Patient recovered.

Aleve Side Effects Report #5658039-4
ALEVE problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 30, 2007. Female patient, 71 years of age, weighting 130.1 lb, was diagnosed with arthralgia and was treated with ALEVE. After drug was administered, patient experienced the following problems/side effects: mouth haemorrhage, . ALEVE dosage: TOTAL DAILY DOSE: 220 MG UNIT DOSE: 220 MG. Patient recovered.

Zometa Side Effects Report #5632962-9
Physician from JAPAN reported ZOMETA problem on Feb 14, 2008. Male patient, 75 years of age, was diagnosed with bone lesion and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: mouth haemorrhage, osteomyelitis, . ZOMETA dosage: 4 MG, QD. During the same period patient was treated with FAMOTIDINE, CONIEL, ROHYPNOL. Patient recovered.

Acetylsalicylic Side Effects Report #5638276-5
ACETYLSALICYLIC ACID SRT problem was reported by a Pharmacist from ITALY on Feb 14, 2008. Female patient, 83 years of age, was diagnosed with thrombosis prophylaxis and was treated with ACETYLSALICYLIC ACID SRT. After drug was administered, patient experienced the following problems/side effects: mouth haemorrhage, . ACETYLSALICYLIC ACID SRT dosage: TOTAL DAILY DOSE: 100 MG UNIT DOSE: 100 MG. Patient recovered.


Listerine Side Effects Report #5583709-6
Consumer or non-health professional from UNITED STATES reported LISTERINE WHITENING QUICK DISSOLVING STRIPS problem on Dec 27, 2007. Female patient was diagnosed with dental care and was treated with LISTERINE WHITENING QUICK DISSOLVING STRIPS. After drug was administered, patient experienced the following problems/side effects: mouth haemorrhage, oral discomfort, . LISTERINE WHITENING QUICK DISSOLVING STRIPS dosage: unknown. Patient recovered.

Zometa Side Effects Report #5572796-7
ZOMETA problem was reported by a Physician from JAPAN on Dec 17, 2007. Male patient, 75 years of age, was diagnosed with bone lesion and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: mouth haemorrhage, osteomyelitis, osteonecrosis, . ZOMETA dosage: 4 MG, QD. During the same period patient was treated with GASTER, CONIEL, ROHYPNOL. Patient recovered.

Commit Side Effects Report #5516625-6
Consumer or non-health professional from UNITED STATES reported COMMIT problem on Mar 29, 2007. Male patient, 24 years of age, was treated with COMMIT. After drug was administered, patient experienced the following problems/side effects: mouth haemorrhage, . COMMIT dosage: unknown. Patient recovered.

Mopral Side Effects Report #5530677-9
MOPRAL problem was reported by a Pharmacist from FRANCE on Nov 27, 2007. Female patient, weighting 103.6 lb, was diagnosed with gastrooesophageal reflux disease, polyarthritis, hypercholesterolaemia and was treated with MOPRAL. After drug was administered, patient experienced the following problems/side effects: mouth haemorrhage, thrombocytopenic purpura, . MOPRAL dosage: unknown. During the same period patient was treated with PREDNISONE, DIFFU K, LODALES. Patient was hospitalized. Patient recovered.

Advair Side Effects Report #5476708-6
Consumer or non-health professional from UNITED STATES reported ADVAIR DISKUS problem on Aug 09, 2007. Male patient, 83 years of age, was diagnosed with chronic obstructive pulmonary disease and was treated with ADVAIR DISKUS. After drug was administered, patient experienced the following problems/side effects: mouth haemorrhage, . ADVAIR DISKUS dosage: unknown. During the same period patient was treated with LIPITOR, ISORDIL, COUMADIN, TOPRAL, ALBUTEROL, IRON SUPPLEMENT. Patient recovered.


Erlotinib Side Effects Report #5501142-X
ERLOTINIB problem was reported by a Physician from UNITED STATES on Oct 11, 2007. Male patient, 74 years of age, weighting 124.1 lb, was diagnosed with non-small cell lung cancer and was treated with ERLOTINIB. After drug was administered, patient experienced the following problems/side effects: mouth haemorrhage, rash, . ERLOTINIB dosage: (150 MG,QD),ORAL; (100 MG,QD), ORAL. During the same period patient was treated with VELCADE, NORTRIPTYLINE, INDOCIN, TETRACYCLINE. Patient died.

Methotrexate Side Effects Report #5385339-8
Pharmacist from UNITED STATES reported METHOTREXATE problem on July 09, 2007. Female patient, 81 years of age, was treated with METHOTREXATE. After drug was administered, patient experienced the following problems/side effects: mouth haemorrhage, mucosal inflammation, respiratory failure, urosepsis, white blood cell count decreased, . METHOTREXATE dosage: unknown. Patient died.

Methotrexate Side Effects Report #5385339-8
METHOTREXATE problem was reported by a Pharmacist from UNITED STATES on July 09, 2007. Female patient, 81 years of age, was treated with METHOTREXATE. After drug was administered, patient experienced the following problems/side effects: mouth haemorrhage, mucosal inflammation, respiratory failure, urosepsis, white blood cell count decreased, . METHOTREXATE dosage: unknown. Patient died.

Concor Side Effects Report #5769160-4
Health Professional from GERMANY reported CONCOR problem on May 29, 2008. Male patient, 54 years of age, was diagnosed with international normalised ratio and was treated with CONCOR. After drug was administered, patient experienced the following problems/side effects: mouth haemorrhage, . CONCOR dosage: (2.5 MG) ORAL. During the same period patient was treated with AMOXICILLIN, COUMADIN. Patient recovered.

Tarceva Side Effects Report #5775257-5
TARCEVA problem was reported by a Consumer or non-health professional from CHINA on May 28, 2008. Male patient, 64 years of age, was diagnosed with metastasis and was treated with TARCEVA. After drug was administered, patient experienced the following problems/side effects: mouth haemorrhage, . TARCEVA dosage: 150 MG, QD, ORAL. Patient died.


Kepivance Side Effects Report #5725076-0
Physician from UNITED STATES reported KEPIVANCE problem on Apr 18, 2008. Female patient, 37 years of age, was diagnosed with mucosal inflammation and was treated with KEPIVANCE. After drug was administered, patient experienced the following problems/side effects: mouth haemorrhage, oropharyngeal blistering, platelet count decreased, . KEPIVANCE dosage: unknown. During the same period patient was treated with CYTOXAN. Patient was hospitalized. Patient recovered.

Nexium Side Effects Report #5722297-8
NEXIUM problem was reported by a Pharmacist from UNITED STATES on July 24, 2007. Female patient, 63 years of age, was treated with NEXIUM. After drug was administered, patient experienced the following problems/side effects: mouth haemorrhage, mouth ulceration, . NEXIUM dosage: unknown. Patient recovered.

Actos Side Effects Report #5722936-1
Consumer or non-health professional from JAPAN reported ACTOS problem on Apr 14, 2008. Female patient, 68 years of age, was diagnosed with diabetes mellitus and was treated with ACTOS. After drug was administered, patient experienced the following problems/side effects: mouth haemorrhage, platelet count decreased, . ACTOS dosage: 7.5 MG (7.5 MG, 1 D) PER ORAL. During the same period patient was treated with AMARYL, SELBEX, ADALAT. Patient was hospitalized. Patient recovered.

Actos Side Effects Report #5727210-5
ACTOS problem was reported by a Consumer or non-health professional from JAPAN on Apr 22, 2008. Female patient, 68 years of age, was diagnosed with diabetes mellitus and was treated with ACTOS. After drug was administered, patient experienced the following problems/side effects: mouth haemorrhage, platelet count decreased, . ACTOS dosage: 7.5 MG (7.5 MG, 1 D) PER ORAL. During the same period patient was treated with AMARYL, SELBEX, ADALAT. Patient was hospitalized. Patient recovered.

Pravastatin Side Effects Report #5359278-2
Health Professional from FRANCE reported PRAVASTATIN problem on June 11, 2007. Male patient, 62 years of age, was treated with PRAVASTATIN. After drug was administered, patient experienced the following problems/side effects: mouth haemorrhage, petechiae, thrombocytopenic purpura, . PRAVASTATIN dosage: unknown. During the same period patient was treated with GLUCOPHAGE, LIPANTHYL, ORACILLINE, DEXAMETHASONE, OMEPRAZOLE, FENOFIBRATE, PHENOXYMETHYL PENICILLIN. Patient was hospitalized. Patient recovered.


Foradil Side Effects Report #5364676-7
FORADIL problem was reported by a Consumer or non-health professional from BRAZIL on June 15, 2007. Male patient, 29 years of age, weighting 198.4 lb, was diagnosed with asthma and was treated with FORADIL. After drug was administered, patient experienced the following problems/side effects: mouth haemorrhage, . FORADIL dosage: unknown. Patient recovered.

Advil Side Effects Report #5314323-5
Consumer or non-health professional from UNITED STATES reported ADVIL problem on Apr 25, 2007. Female patient was diagnosed with arthritis, headache and was treated with ADVIL. After drug was administered, patient experienced the following problems/side effects: mouth haemorrhage, overdose, . ADVIL dosage: unknown. Patient died on 01/01/2001.

Alimta Side Effects Report #5321911-9
ALIMTA problem was reported by a Health Professional from UNITED STATES on May 08, 2007. Male patient, weighting 146.0 lb, was diagnosed with neoplasm malignant and was treated with ALIMTA. After drug was administered, patient experienced the following problems/side effects: mouth haemorrhage, . ALIMTA dosage: 895 MG/IV EVERY 3 WEEKS. During the same period patient was treated with AVASTIN. Patient was hospitalized. Patient recovered.

Alimta Side Effects Report #5321912-0
Health Professional from UNITED STATES reported ALIMTA problem on May 08, 2007. Male patient, weighting 146.0 lb, was diagnosed with neoplasm malignant and was treated with ALIMTA. After drug was administered, patient experienced the following problems/side effects: mouth haemorrhage, . ALIMTA dosage: 895 MG IV /EVERY 3 WEEKS. During the same period patient was treated with AVASTIN. Patient was hospitalized. Patient recovered.

Plavix Side Effects Report #5331882-7
PLAVIX problem was reported by a Physician from UNITED STATES on June 22, 2006. Male patient was treated with PLAVIX. After drug was administered, patient experienced the following problems/side effects: mouth haemorrhage, . PLAVIX dosage: unknown. Patient was hospitalized. Patient recovered.

Plavix Side Effects Report #5331883-9
Physician from UNITED STATES reported PLAVIX problem on June 22, 2006. Male patient was treated with PLAVIX. After drug was administered, patient experienced the following problems/side effects: mouth haemorrhage, . PLAVIX dosage: unknown. Patient was hospitalized. Patient recovered.

Remicade Side Effects Report #5253974-3
REMICADE problem was reported by a Health Professional from SWEDEN on Feb 23, 2007. Male patient, 87 years of age, was diagnosed with rheumatoid arthritis and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: mouth haemorrhage, pancytopenia, . REMICADE dosage: unknown. During the same period patient was treated with METHOTREXATE, DICLOFENAC, FOLACIN, PANODIL, PREDNISOLONE, CALCIPOS. Patient was hospitalized. Patient recovered.

Boniva Side Effects Report #5627939-3
Consumer or non-health professional from GERMANY reported BONIVA problem on Feb 05, 2008. Female patient, 79 years of age, was diagnosed with osteoporosis and was treated with BONIVA. After drug was administered, patient experienced the following problems/side effects: epistaxis, mouth haemorrhage, rectal haemorrhage, . BONIVA dosage: unknown. During the same period patient was treated with ASPIRIN, PLAVIX, AGRYLIN, NEXIUM. Patient was hospitalized. Patient recovered.

Cilostazol Side Effects Report #5564237-0
CILOSTAZOL problem was reported by a Consumer or non-health professional from JAPAN on Nov 28, 2007. Male patient, 85 years of age, was diagnosed with peripheral circulatory failure and was treated with CILOSTAZOL. After drug was administered, patient experienced the following problems/side effects: leukoplakia oesophageal, mouth haemorrhage, oesophageal haemorrhage, oral mucosal exfoliation, renal failure, . CILOSTAZOL dosage: 200 MG, ORAL. During the same period patient was treated with FUROSEMIDE, AMLODIPINE BESYLATE, ALFACALCIDOL, ZOPICLONE, LANSOPRAZOLE, ASCORBIC ACID, ALPROSTADIL, DARBEPOETIN ALFA. Patient was hospitalized. Patient recovered.

Boniva Side Effects Report #5570892-1
Consumer or non-health professional from UNITED STATES reported BONIVA problem on Dec 10, 2007. Female patient, 79 years of age, was diagnosed with osteoporosis and was treated with BONIVA. After drug was administered, patient experienced the following problems/side effects: epistaxis, mouth haemorrhage, rectal haemorrhage, . BONIVA dosage: unknown. During the same period patient was treated with ASPIRIN, PLAVIX, AGRYLIN, NEXIUM. Patient was hospitalized. Patient recovered.

Exelon Side Effects Report #5572784-0
EXELON problem was reported by a Consumer or non-health professional from NETHERLANDS on Dec 13, 2007. Female patient, 79 years of age, was diagnosed with hallucination, visual, constipation and was treated with EXELON. After drug was administered, patient experienced the following problems/side effects: mouth haemorrhage, . EXELON dosage: 1.5 MG, QD. During the same period patient was treated with ACETYLSALICYLIC ACID SRT, ACTRAPID, COLEX, LIDOCAINE, VASELINE, METFORMIN, MIRTAZAPINE. Patient recovered.

Exelon Side Effects Report #5576121-7
Consumer or non-health professional from NETHERLANDS reported EXELON problem on Dec 20, 2007. Female patient, 79 years of age, was diagnosed with hallucination, visual, constipation and was treated with EXELON. After drug was administered, patient experienced the following problems/side effects: mouth haemorrhage, . EXELON dosage: 1.5 MG, QD. During the same period patient was treated with ACETYLSALICYLIC ACID SRT, ACTRAPID, COLEX, LIDOCAINE, VASELINE, METFORMIN, MIRTAZAPINE. Patient recovered.

Erlotinib Side Effects Report #5506948-9
ERLOTINIB problem was reported by a Health Professional from UNITED STATES on Oct 19, 2007. Female patient, 48 years of age, weighting 102.1 lb, was diagnosed with non-small cell lung cancer and was treated with ERLOTINIB. After drug was administered, patient experienced the following problems/side effects: electromechanical dissociation, mouth haemorrhage, pulmonary haemorrhage, thrombosis, . ERLOTINIB dosage: 150 MG, QD), ORAL. During the same period patient was treated with BEVACIZUMAB. Patient died on 09/28/2007.

Avodart Side Effects Report #5514589-2
Consumer or non-health professional from SPAIN reported AVODART problem on Nov 08, 2007. Male patient, 82 years of age, was diagnosed with benign prostatic hyperplasia and was treated with AVODART. After drug was administered, patient experienced the following problems/side effects: hypertensive crisis, mouth haemorrhage, . AVODART dosage: .5MG PER DAY. Patient recovered.

Raptiva Side Effects Report #5515240-8
RAPTIVA problem was reported by a Physician from SWITZERLAND on Nov 08, 2007. Male patient was diagnosed with psoriasis and was treated with RAPTIVA. After drug was administered, patient experienced the following problems/side effects: autoimmune thrombocytopenia, mouth haemorrhage, . RAPTIVA dosage: 100 MG, 1/WEEK. Patient was hospitalized. Patient recovered.

Fosamax Side Effects Report #5524131-8
Health Professional from UNITED KINGDOM reported FOSAMAX problem on Nov 16, 2007. Female patient, 96 years of age, was diagnosed with osteoporosis, pollakiuria, urinary tract infection and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: decreased appetite, mouth haemorrhage, oral mucosal blistering, oral pain, swelling face, . FOSAMAX dosage: unknown. During the same period patient was treated with CALCIUM CARBONATE AND CHOLECALCIFEROL, OXYBUTYNIN, TRIMETHOPRIM. Patient recovered.

Boniva Side Effects Report #5530350-7
BONIVA problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 19, 2007. Female patient, 79 years of age, was diagnosed with osteoporosis and was treated with BONIVA. After drug was administered, patient experienced the following problems/side effects: epistaxis, mouth haemorrhage, rectal haemorrhage, . BONIVA dosage: unknown. During the same period patient was treated with ASPIRIN, PLAVIX, AGRYLIN, NEXIUM. Patient was hospitalized. Patient recovered.

Cilostazol Side Effects Report #5531362-X
Consumer or non-health professional from JAPAN reported CILOSTAZOL problem on Nov 13, 2007. Male patient, 85 years of age, was diagnosed with peripheral circulatory failure and was treated with CILOSTAZOL. After drug was administered, patient experienced the following problems/side effects: leukoplakia, mouth haemorrhage, . CILOSTAZOL dosage: 200 MG ORAL. During the same period patient was treated with ASCORBIC ACID, ALPROSTADIL, DARBEPOETIN ALFA, FERRIC OXIDE SACCHARATED, ZOPICLONE, SENNOSIDE, LANSOPRAZOLE, FUROSEMIDE. Patient was hospitalized. Patient recovered.

Argatroban Side Effects Report #5534045-5
ARGATROBAN problem was reported by a Pharmacist from UNITED STATES on Nov 29, 2007. Male patient, 90 years of age, weighting 160.0 lb, was treated with ARGATROBAN. After drug was administered, patient experienced the following problems/side effects: ear haemorrhage, mouth haemorrhage, . ARGATROBAN dosage: unknown. Patient recovered.

Velcade Side Effects Report #5500134-4
Pharmacist from UNITED KINGDOM reported VELCADE problem on Oct 15, 2007. Female patient, 59 years of age, was diagnosed with leukaemia plasmacytic and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, mouth haemorrhage, platelet count decreased, . VELCADE dosage: unknown. Patient recovered.

Raptiva Side Effects Report #5459118-7
RAPTIVA problem was reported by a Physician from SWITZERLAND on Sept 14, 2007. Male patient was diagnosed with psoriasis and was treated with RAPTIVA. After drug was administered, patient experienced the following problems/side effects: autoimmune thrombocytopenia, mouth haemorrhage, . RAPTIVA dosage: 100 MG, 1/WEEK. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5379225-7
Physician from GERMANY reported SUTENT problem on June 26, 2007. Female patient, weighting 143.3 lb, was diagnosed with gastrointestinal stromal tumour and was treated with SUTENT. After drug was administered, patient experienced the following problems/side effects: epistaxis, mouth haemorrhage, swollen tongue, . SUTENT dosage: DAILY DOSE:37.5MG. During the same period patient was treated with GLEEVEC. Patient recovered.

Cytarabine Side Effects Report #5392147-0
CYTARABINE problem was reported by a Consumer or non-health professional from UNITED STATES on July 18, 2007. Female patient, weighting 167.3 lb, was treated with CYTARABINE. After drug was administered, patient experienced the following problems/side effects: epistaxis, mouth haemorrhage, platelet count abnormal, skin haemorrhage, . CYTARABINE dosage: 16650 MG. Patient recovered.

Sutent Side Effects Report #5379225-7
Physician from GERMANY reported SUTENT problem on June 26, 2007. Female patient, weighting 143.3 lb, was diagnosed with gastrointestinal stromal tumour and was treated with SUTENT. After drug was administered, patient experienced the following problems/side effects: epistaxis, mouth haemorrhage, swollen tongue, . SUTENT dosage: DAILY DOSE:37.5MG. During the same period patient was treated with GLEEVEC. Patient recovered.

Cytarabine Side Effects Report #5392147-0
CYTARABINE problem was reported by a Consumer or non-health professional from UNITED STATES on July 18, 2007. Female patient, weighting 167.3 lb, was treated with CYTARABINE. After drug was administered, patient experienced the following problems/side effects: epistaxis, mouth haemorrhage, platelet count abnormal, skin haemorrhage, . CYTARABINE dosage: 16650 MG. Patient recovered.

Reopro Side Effects Report #5756480-2
Physician from MEXICO reported REOPRO problem on May 28, 2008. Male patient, 47 years of age, weighting 198.4 lb, was treated with REOPRO. After drug was administered, patient experienced the following problems/side effects: mouth haemorrhage, musculoskeletal chest pain, myocardial infarction, pharmaceutical product counterfeit, . REOPRO dosage: 17 ML/HR, THEN INCREASING TO 24 ML/HR UP TO 28 ML/HR. During the same period patient was treated with HEPARIN, FENTANYL TRANSDERMAL SYSTEM, MIDAZOLAM. Patient was hospitalized. Patient died on 04/28/2008.

Pulmicort Side Effects Report #5758954-7
PULMICORT problem was reported by a Health Professional from FINLAND on May 30, 2008. Male patient was diagnosed with asthma, cough, dyspnoea, stridor and was treated with PULMICORT. After drug was administered, patient experienced the following problems/side effects: gingival hyperplasia, mouth haemorrhage, oral mucosa erosion, . PULMICORT dosage: unknown. During the same period patient was treated with AIROMIR. Patient recovered.

Pulmicort Side Effects Report #5774123-9
Health Professional from FINLAND reported PULMICORT problem on June 10, 2008. Male patient was diagnosed with asthma, cough, dyspnoea, stridor and was treated with PULMICORT. After drug was administered, patient experienced the following problems/side effects: gingival hyperplasia, mouth haemorrhage, oral mucosa erosion, . PULMICORT dosage: unknown. During the same period patient was treated with AIROMIR, SINGULAIR. Patient recovered.

Reopro Side Effects Report #5787035-1
REOPRO problem was reported by a Physician from MEXICO on June 23, 2008. Male patient, 47 years of age, weighting 198.4 lb, was treated with REOPRO. After drug was administered, patient experienced the following problems/side effects: mouth haemorrhage, musculoskeletal chest pain, myocardial infarction, pharmaceutical product counterfeit, . REOPRO dosage: 17 ML/HR, THEN INCREASING TO 24 ML/HR UP TO 28 ML/HR. During the same period patient was treated with HEPARIN, FENTANYL, MIDAZOLAM. Patient was hospitalized. Patient died on 04/28/2008.

Aldara Side Effects Report #5789383-8
Pharmacist from UNITED STATES reported ALDARA problem on June 25, 2008. Male patient, 94 years of age, weighting 116.8 lb, was diagnosed with basal cell carcinoma and was treated with ALDARA. After drug was administered, patient experienced the following problems/side effects: idiopathic thrombocytopenic purpura, mouth haemorrhage, . ALDARA dosage: unknown. Patient was hospitalized. Patient recovered.

Reopro Side Effects Report #5731364-4
REOPRO problem was reported by a Physician from MEXICO on Apr 30, 2008. Male patient, 47 years of age, weighting 198.4 lb, was treated with REOPRO. After drug was administered, patient experienced the following problems/side effects: mouth haemorrhage, musculoskeletal chest pain, myocardial infarction, . REOPRO dosage: 17 ML/HR, THEN INCREASING TO 24 ML/HR UP TO 28 ML/HR. During the same period patient was treated with HEPARIN, FENTANYL, MIDAZOLAM. Patient was hospitalized. Patient died on 04/28/2008.

Reopro Side Effects Report #5740078-6
Physician from MEXICO reported REOPRO problem on May 13, 2008. Male patient, 47 years of age, weighting 198.4 lb, was treated with REOPRO. After drug was administered, patient experienced the following problems/side effects: mouth haemorrhage, musculoskeletal chest pain, myocardial infarction, pharmaceutical product counterfeit, . REOPRO dosage: 17 ML/HR, THEN INCREASING TO 24 ML/HR UP TO 28 ML/HR. During the same period patient was treated with HEPARIN, FENTANYL CITRATE, MIDAZOLAM. Patient was hospitalized. Patient died on 04/28/2008.