The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
106802423 10680242 3 F 200905 20160801 20141229 20160812 EXP US-SA-2013SA122575 AVENTIS 50.00 YR A F Y 63.50000 KG 20160812 MD US US

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
106802423 10680242 1 PS PLAVIX CLOPIDOGREL BISULFATE 1 Unknown FIRST DATE:2003 OR 2005 UNKNOWN 20839 75 MG TABLET QD
106802423 10680242 2 SS PLAVIX CLOPIDOGREL BISULFATE 1 Unknown FIRST DATE:2003 OR 2005 UNKNOWN 20839 75 MG TABLET QD
106802423 10680242 3 SS PLAVIX CLOPIDOGREL BISULFATE 1 Unknown UNK 20839 75 MG TABLET QD
106802423 10680242 4 SS PLAVIX CLOPIDOGREL BISULFATE 1 Unknown UNK 20839 75 MG TABLET QD
106802423 10680242 5 SS PLAVIX CLOPIDOGREL BISULFATE 1 Oral UNK 20839 75 MG TABLET QD
106802423 10680242 6 SS PLAVIX CLOPIDOGREL BISULFATE 1 Oral UNK 20839 75 MG TABLET QD
106802423 10680242 7 C ASPIRIN. ASPIRIN 1 Unknown UNK 0 81 G QD
106802423 10680242 8 C ASPIRIN. ASPIRIN 1 Unknown 0 325 MG
106802423 10680242 9 C ABCIXIMAB ABCIXIMAB 1 0
106802423 10680242 10 C EPTIFIBATIDE. EPTIFIBATIDE 1 0
106802423 10680242 11 C TIROFIBAN TIROFIBAN 1 0
106802423 10680242 12 C TICLOPIDINE TICLOPIDINE 1 0
106802423 10680242 13 C AGGRENOX ASPIRINDIPYRIDAMOLE 1 0
106802423 10680242 14 C EFFIENT PRASUGREL HYDROCHLORIDE 1 0
106802423 10680242 15 C BRILINTA TICAGRELOR 1 0
106802423 10680242 16 C CIMETIDINE CIMETIDINE 1 0
106802423 10680242 17 C ZANTAC RANITIDINE HYDROCHLORIDE 1 0
106802423 10680242 18 C ZOCOR SIMVASTATIN 1 0
106802423 10680242 19 C LIPITOR ATORVASTATIN CALCIUM 1 0
106802423 10680242 20 C PRILOSEC OMEPRAZOLE MAGNESIUM 1 0
106802423 10680242 21 C PREVACID LANSOPRAZOLE 1 0
106802423 10680242 22 C ACIPHEX RABEPRAZOLE SODIUM 1 0
106802423 10680242 23 C PROTONIX PANTOPRAZOLE SODIUM 1 0
106802423 10680242 24 C NEXIUM ESOMEPRAZOLE MAGNESIUM 1 0
106802423 10680242 25 C ZEGERID OMEPRAZOLESODIUM BICARBONATE 1 0
106802423 10680242 26 C TYLENOL ACETAMINOPHEN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
106802423 10680242 1 Arterial occlusive disease
106802423 10680242 2 Stent placement
106802423 10680242 3 Arterial occlusive disease
106802423 10680242 4 Stent placement
106802423 10680242 5 Arterial occlusive disease
106802423 10680242 6 Stent placement

Outcome of event

Event ID CASEID OUTC COD
106802423 10680242 DE
106802423 10680242 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
106802423 10680242 Anaemia
106802423 10680242 Angina unstable
106802423 10680242 Dyspnoea
106802423 10680242 Gastrointestinal haemorrhage
106802423 10680242 Haemoptysis
106802423 10680242 Impaired healing
106802423 10680242 Intermittent claudication
106802423 10680242 Melaena
106802423 10680242 Pleurisy
106802423 10680242 Pneumonia
106802423 10680242 Respiratory failure
106802423 10680242 Syncope

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
106802423 10680242 1 2002 2005 0
106802423 10680242 2 2002 2005 0
106802423 10680242 3 2006 0
106802423 10680242 4 2006 0
106802423 10680242 7 2004 0