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
125678361 12567836 1 I 20160710 20160715 20160718 20160718 EXP US-MYLANLABS-2016M1029565 MYLAN 0.00 Y 0.00000 20160718 PH 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
125678361 12567836 1 PS FENTANYL TRANSDERMAL SYSTEM FENTANYL 1 Transdermal 50 ?G, QH, CHANGE Q72H 615214 76258 50 UG TRANSDERMAL PATCH /hr

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125678361 12567836 1 Pain

Outcome of event

Event ID CASEID OUTC COD
125678361 12567836 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125678361 12567836 Drug ineffective
125678361 12567836 Withdrawal syndrome

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

no results found

Therapies reported

no results found