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
125215491 12521549 1 I 20160624 20160701 20160701 EXP CA-JNJFOC-20160622657 JANSSEN 2.00 DEC T F Y 0.00000 20160701 CN CA CA

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
125215491 12521549 1 PS FENTANYL. FENTANYL 1 Unknown Y N 19813 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125215491 12521549 1 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125215491 12521549 HO
125215491 12521549 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125215491 12521549 Abdominal pain upper
125215491 12521549 Drug dependence
125215491 12521549 Drug diversion
125215491 12521549 Drug withdrawal syndrome
125215491 12521549 Hypoaesthesia
125215491 12521549 Insomnia
125215491 12521549 Loss of consciousness
125215491 12521549 Muscle twitching
125215491 12521549 Overdose
125215491 12521549 Pain
125215491 12521549 Psychomotor hyperactivity
125215491 12521549 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
125215491 12521549 1 20151002 0