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
125903182 12590318 2 F 20141024 20160831 20160725 20160901 EXP US-ALLERGAN-1663626US ALLERGAN 31.00 YR M Y 86.20000 KG 20160901 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
125903182 12590318 1 PS NORCO ACETAMINOPHENHYDROCODONE BITARTRATE 1 U U 40148 TABLET
125903182 12590318 2 SS LUNESTA ESZOPICLONE 1 Oral 3 MG, QHS Y Y 0 3 MG QD
125903182 12590318 3 SS LYRICA PREGABALIN 1 300 MG, BID Y Y 0 300 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125903182 12590318 1 Back pain
125903182 12590318 2 Insomnia
125903182 12590318 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125903182 12590318 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125903182 12590318 Brain injury
125903182 12590318 Cognitive disorder
125903182 12590318 Sedation

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
125903182 12590318 2 20141024 0