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
125559812 12555981 2 F 20160721 20160714 20160726 EXP JP-JNJFOC-20160707297 JANSSEN YAMAMOTO K. WITHDRAWAL SYMPTOMS DURING TRANSDERMAL THERAPEUTIC SYSTEM OF FENTANYL: A CASE REPORT. JOURNAL OF JAPAN SOCIETY OF PAIN CLINICIANS JUN-2016;23(3):463; G1621450. 5.00 DEC A M Y 0.00000 20160726 MD JP JP

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
125559812 12555981 1 SS DUROTEP MT FENTANYL 1 Transdermal 4.0 MG PER DAY N 0 MATRIX PATCH
125559812 12555981 2 PS DUROTEP MT FENTANYL 1 Transdermal 5.0 MG PER DAY N 19813 MATRIX PATCH
125559812 12555981 3 SS FENTANYL. FENTANYL 1 Transdermal 4.0 MG PER DAY Y 0 MATRIX PATCH
125559812 12555981 4 SS FENTANYL. FENTANYL 1 Transdermal 5.0 MG PER DAY Y 0 MATRIX PATCH

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125559812 12555981 1 Pain
125559812 12555981 2 Pain
125559812 12555981 3 Pain
125559812 12555981 4 Pain

Outcome of event

Event ID CASEID OUTC COD
125559812 12555981 OT
125559812 12555981 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125559812 12555981 Agitation
125559812 12555981 Application site dryness
125559812 12555981 Chills
125559812 12555981 Hyperhidrosis
125559812 12555981 Irritability
125559812 12555981 Pain in extremity
125559812 12555981 Salivary hypersecretion
125559812 12555981 Tremor
125559812 12555981 Withdrawal syndrome

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found