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
125312723 12531272 3 F 2016 20160809 20160706 20160907 PER US-JNJFOC-20160702412 JANSSEN 0.00 E F Y 72.58000 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
125312723 12531272 1 SS DURAGESIC FENTANYL 1 Transdermal N 1509824P1 0 75 UG PATCH
125312723 12531272 2 SS DURAGESIC FENTANYL 1 Transdermal STOPPED IN 2016 N 1509824P1 0 PATCH
125312723 12531272 3 SS DURAGESIC FENTANYL 1 Transdermal STOPPED IN 2016 N 1509824P1 0 PATCH
125312723 12531272 4 PS DURAGESIC FENTANYL 1 Transdermal STOPPED IN PREVIOUS YEARS FROM THE TIME OF REPORT N 1509824P1 19813 75 UG PATCH

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125312723 12531272 1 Intervertebral disc protrusion
125312723 12531272 2 Intervertebral disc protrusion
125312723 12531272 3 Intervertebral disc protrusion
125312723 12531272 4 Intervertebral disc protrusion

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125312723 12531272 Adverse event
125312723 12531272 Drug dose omission
125312723 12531272 Hyperhidrosis
125312723 12531272 Pain
125312723 12531272 Product adhesion issue
125312723 12531272 Withdrawal syndrome
125312723 12531272 Wrong technique in product usage process

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
125312723 12531272 2 2016 0
125312723 12531272 3 2016 0
125312723 12531272 4 2013 0