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
100235201 10023520 1 I 201310 20131219 20131231 20131231 EXP E2B_7258859 MERCK KGAA 70.00 YR F N 0.00000 20131227 N OT ES

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
100235201 10023520 1 PS EUTIROX 1 ORAL D D 21292 25 UG QD
100235201 10023520 3 C METFORMIN (METFORMIN) (METFORMIN) 1 0
100235201 10023520 5 C FOLI DOCE (FOLGAMMA /00349401/) (FOLIC ACID CYANOCOBALAMIN) 2 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
100235201 10023520 1 Hypothyroidism

Outcome of event

Event ID CASEID OUTC COD
100235201 10023520 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
100235201 10023520 Balance disorder
100235201 10023520 Chest pain
100235201 10023520 Myalgia

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

Event ID CASEID RPSR COD
100235201 10023520 FGN
100235201 10023520 HP

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
100235201 10023520 1 20131028 20131107 11 DAY