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
126947012 12694701 2 F 201607 20160831 20160829 20160905 EXP US-JNJFOC-20160814029 JANSSEN 54.92 YR A M Y 81.65000 KG 20160905 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
126947012 12694701 1 SS DURAGESIC FENTANYL 1 Transdermal N UNKNOWN 0 UNSPECIFIED
126947012 12694701 2 SS DURAGESIC FENTANYL 1 Transdermal N UNKNOWN 0 UNSPECIFIED
126947012 12694701 3 PS DURAGESIC FENTANYL 1 Transdermal N UNKNOWN 19813 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126947012 12694701 1 Spinal pain
126947012 12694701 2 Spinal pain
126947012 12694701 3 Spinal pain

Outcome of event

Event ID CASEID OUTC COD
126947012 12694701 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126947012 12694701 Arachnoiditis
126947012 12694701 Clavicle fracture
126947012 12694701 Drug ineffective
126947012 12694701 Drug tolerance
126947012 12694701 Fall
126947012 12694701 Melanoma recurrent
126947012 12694701 Muscle spasticity
126947012 12694701 Pain
126947012 12694701 Rib fracture
126947012 12694701 Spinal disorder

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
126947012 12694701 3 2002 0