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
126649601 12664960 1 I 20160427 20160810 20160818 20160818 EXP JP-SA-2016SA149465 AVENTIS 81.00 YR E F Y 49.00000 KG 20160818 PH JP JP

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
126649601 12664960 1 PS PLAVIX CLOPIDOGREL BISULFATE 1 Oral UNK 20839 1 DF TABLET QD
126649601 12664960 2 SS ADALAT NIFEDIPINE 1 Oral UNK 0 20 MG CAPSULE QD
126649601 12664960 3 SS ARGATROBAN. ARGATROBAN 1 Intravenous (not otherwise specified) UNK 0
126649601 12664960 4 SS EDARAVONE EDARAVONE 1 Intravenous (not otherwise specified) UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126649601 12664960 1 Thrombolysis
126649601 12664960 2 Blood pressure increased
126649601 12664960 3 Brain stem infarction
126649601 12664960 4 Brain stem infarction

Outcome of event

Event ID CASEID OUTC COD
126649601 12664960 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
126649601 12664960 Drug eruption

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
126649601 12664960 1 20160424 20160505 0
126649601 12664960 2 20160425 20160428 0
126649601 12664960 3 20160422 20160428 0
126649601 12664960 4 20160422 20160505 0