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
74180892 7418089 2 F 2010 20160826 20100614 20160829 EXP US-JNJFOC-20100602612 JANSSEN 71.64 YR E M Y 68.04000 KG 20160829 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
74180892 7418089 1 SS FENTANYL TRANSDERMAL SYSTEM FENTANYL 1 Transdermal N UNKNOWN;UNKNOWN 0 MATRIX PATCH
74180892 7418089 2 SS FENTANYL TRANSDERMAL SYSTEM FENTANYL 1 Transdermal N UNKNOWN;UNKNOWN 0 MATRIX PATCH
74180892 7418089 3 PS FENTANYL TRANSDERMAL SYSTEM FENTANYL 1 Transdermal N UNKNOWN;UNKNOWN 19813 MATRIX PATCH
74180892 7418089 4 C NORCO ACETAMINOPHENHYDROCODONE BITARTRATE 1 Oral 10/325MG/ 1-2 AS NEEDED 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
74180892 7418089 1 Pain
74180892 7418089 2 Pain
74180892 7418089 3 Pain
74180892 7418089 4 Breakthrough pain

Outcome of event

Event ID CASEID OUTC COD
74180892 7418089 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
74180892 7418089 Adverse event
74180892 7418089 Anxiety
74180892 7418089 Application site pruritus
74180892 7418089 Catheter placement
74180892 7418089 Drug ineffective
74180892 7418089 Metastases to lymph nodes
74180892 7418089 Nausea

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
74180892 7418089 1 20100603 0
74180892 7418089 2 201004 0
74180892 7418089 3 2010 20100603 0