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
125484442 12548444 2 F 20160808 20160712 20160816 EXP US-JNJFOC-20160707095 JANSSEN 0.00 A M Y 104.33000 KG 20160816 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
125484442 12548444 1 PS FENTANYL. FENTANYL 1 Transdermal INITIATED ABOUT 5-7 YEARS AGO. N UNKNOWN;UNKNOWN 19813 125 UG PATCH QOD
125484442 12548444 2 SS LORTAB ACETAMINOPHENHYDROCODONE BITARTRATE 1 Oral U 0 10 MG TABLET TID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125484442 12548444 1 Arthralgia
125484442 12548444 2 Breakthrough pain

Outcome of event

Event ID CASEID OUTC COD
125484442 12548444 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125484442 12548444 Abasia
125484442 12548444 Breakthrough pain
125484442 12548444 Drug dose omission
125484442 12548444 Nephropathy
125484442 12548444 Product quality issue
125484442 12548444 Underdose
125484442 12548444 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
125484442 12548444 1 2016 0