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
122070692 12207069 2 F 2010 20160303 20160324 20160907 PER US-JNJFOC-20160304724 JANSSEN 0.00 A F Y 39.46000 KG 20160907 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
122070692 12207069 1 SS FENTANYL TRANSDERMAL SYSTEM FENTANYL 1 Transdermal N UNKNOWN 0 MATRIX PATCH
122070692 12207069 2 PS FENTANYL TRANSDERMAL SYSTEM FENTANYL 1 Transdermal N UNKNOWN 19813 MATRIX PATCH

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122070692 12207069 1 Pain
122070692 12207069 2 Pain

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
122070692 12207069 Abnormal loss of weight
122070692 12207069 Activities of daily living impaired
122070692 12207069 Condition aggravated
122070692 12207069 Drug ineffective
122070692 12207069 Feeding 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
122070692 12207069 1 2013 0
122070692 12207069 2 2010 2013 0