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
124339093 12433909 3 F 20160914 20160603 20160926 EXP GB-SA-2016SA102815 AVENTIS 90.00 YR E M Y 0.00000 20160926 OT GB GB

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
124339093 12433909 1 PS CLOPIDOGREL BISULFATE. CLOPIDOGREL BISULFATE 1 Oral UNK 20839 75 MG
124339093 12433909 2 SS CLOPIDOGREL BISULFATE. CLOPIDOGREL BISULFATE 1 Oral UNK 20839 75 MG
124339093 12433909 3 SS CLOPIDOGREL BISULFATE. CLOPIDOGREL BISULFATE 1 Oral UNK 20839 75 MG
124339093 12433909 4 SS APIXABAN APIXABAN 1 Oral UNK 0 2.5 MG BID
124339093 12433909 5 SS APIXABAN APIXABAN 1 Oral UNK 0 2.5 MG BID
124339093 12433909 6 SS APIXABAN APIXABAN 1 Oral UNK 0 2.5 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124339093 12433909 1 Prophylaxis
124339093 12433909 2 Atrial fibrillation
124339093 12433909 3 Heart valve replacement
124339093 12433909 4 Atrial fibrillation
124339093 12433909 5 Prophylaxis
124339093 12433909 6 Cerebrovascular accident prophylaxis

Outcome of event

Event ID CASEID OUTC COD
124339093 12433909 OT
124339093 12433909 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124339093 12433909 Cerebrovascular accident
124339093 12433909 Contraindicated product administered
124339093 12433909 Deep vein thrombosis
124339093 12433909 Haematoma
124339093 12433909 Muscle haemorrhage
124339093 12433909 Transcatheter aortic valve implantation
124339093 12433909 Transfusion

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

no results found

Therapies reported

no results found