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
126510301 12651030 1 I 20160808 0 20160812 20160812 DIR 61.00 YR F N 155.00000 LBS 20160811 N 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
126510301 12651030 1 PS AGGRENOX ASPIRINDIPYRIDAMOLE 1 Oral Y D 0 QD
126510301 12651030 3 C CELEXA CITALOPRAM HYDROBROMIDE 1 0
126510301 12651030 5 C WELLBUTRIN BUPROPION HYDROCHLORIDE 1 0
126510301 12651030 7 C REQUIP ROPINIROLE HYDROCHLORIDE 1 0
126510301 12651030 9 C LIPITOR ATORVASTATIN CALCIUM 1 0
126510301 12651030 11 C ASPIRIN. ASPIRIN 1 0
126510301 12651030 13 C MULTI VITAMIN VITAMINS 1 0
126510301 12651030 15 C VALARIUM ROOT 2 0
126510301 12651030 17 C VITAMIN D CHOLECALCIFEROL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126510301 12651030 1 Thrombosis prophylaxis

Outcome of event

Event ID CASEID OUTC COD
126510301 12651030 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126510301 12651030 Migraine
126510301 12651030 Nausea
126510301 12651030 Vomiting

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
126510301 12651030 1 20160808 20160808 0