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
126643422 12664342 2 F 2009 20160916 20160818 20160920 EXP US-JNJFOC-20160811050 JANSSEN 59.73 YR A F Y 83.92000 KG 20160920 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
126643422 12664342 1 PS DURAGESIC FENTANYL 1 Transdermal N 1509761P1 19813 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126643422 12664342 1 Pain management

Outcome of event

Event ID CASEID OUTC COD
126643422 12664342 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126643422 12664342 Amnesia
126643422 12664342 Gallbladder operation
126643422 12664342 Hypertension
126643422 12664342 Ligament operation
126643422 12664342 Medical device implantation
126643422 12664342 Product adhesion issue
126643422 12664342 Rotator cuff repair
126643422 12664342 Spinal osteoarthritis
126643422 12664342 Type 2 diabetes mellitus
126643422 12664342 Withdrawal syndrome
126643422 12664342 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

no results found