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
126869601 12686960 1 I 20160507 20160811 20160826 20160826 EXP IT-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-122353 RANBAXY 20.18 YR F Y 0.00000 20160826 OT IT IT

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
126869601 12686960 1 SS HALDOL HALOPERIDOL 1 Oral 2 MG DAILY Y U 0 2 MG
126869601 12686960 2 PS SERTRALINE HYDROCHLORIDE. SERTRALINE HYDROCHLORIDE 1 Oral 50 MG DAILY Y U 77977 50 MG TABLET
126869601 12686960 3 C ALPRAZOLAM. ALPRAZOLAM 1 Oral 10 GTT U U 0 10 GTT

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126869601 12686960 1 Psychotic disorder
126869601 12686960 2 Psychotic disorder
126869601 12686960 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126869601 12686960 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126869601 12686960 Confusional state
126869601 12686960 Extrapyramidal disorder
126869601 12686960 Joint stiffness
126869601 12686960 Tremor

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
126869601 12686960 1 20160506 20160510 0
126869601 12686960 2 20160506 20160510 0