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
115106752 11510675 2 F 2014 20150910 20150915 20160712 EXP US-JNJFOC-20150909521 JANSSEN 58.33 YR A M Y 113.40000 KG 20160712 CN 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
115106752 11510675 1 SS FENTANYL TRANSDERMAL SYSTEM FENTANYL 1 Transdermal Y N UNKNOWN;UNKNOWN;1405003P1 0 MATRIX PATCH
115106752 11510675 2 SS FENTANYL TRANSDERMAL SYSTEM FENTANYL 1 Transdermal Y N UNKNOWN;UNKNOWN;1405003P1 0 MATRIX PATCH
115106752 11510675 3 PS FENTANYL TRANSDERMAL SYSTEM FENTANYL 1 Transdermal Y N UNKNOWN;UNKNOWN;1405003P1 19813 MATRIX PATCH

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
115106752 11510675 1 Pain
115106752 11510675 2 Pain
115106752 11510675 3 Pain

Outcome of event

Event ID CASEID OUTC COD
115106752 11510675 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
115106752 11510675 Activities of daily living impaired
115106752 11510675 Drug ineffective
115106752 11510675 Hypersomnia
115106752 11510675 Myocardial infarction
115106752 11510675 Product quality issue

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
115106752 11510675 1 2014 2014 0
115106752 11510675 2 20150901 0
115106752 11510675 3 2014 201406 0