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
109660572 10966057 2 F 20140930 20141104 20150330 20160729 EXP US-MYLANLABS-2014M1006685 MYLAN 0.00 Y 0.00000 20160729 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
109660572 10966057 1 PS FENTANYL TRANSDERMAL SYSTEM FENTANYL 1 Transdermal 100 ?G, QH, EVERY 48 HOURS 2400 UG Y 614008 76258 100 UG TRANSDERMAL PATCH /hr

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
109660572 10966057 1 Pain

Outcome of event

Event ID CASEID OUTC COD
109660572 10966057 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
109660572 10966057 Chills
109660572 10966057 Confusional state
109660572 10966057 Dizziness
109660572 10966057 Drug effect increased
109660572 10966057 Fatigue
109660572 10966057 Feeling drunk
109660572 10966057 Gait disturbance
109660572 10966057 Headache
109660572 10966057 Hyperhidrosis
109660572 10966057 Mental impairment
109660572 10966057 Nausea
109660572 10966057 Presyncope
109660572 10966057 Pruritus
109660572 10966057 Sedation
109660572 10966057 Somnolence
109660572 10966057 Speech disorder
109660572 10966057 Vomiting
109660572 10966057 Withdrawal syndrome
109660572 10966057 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
109660572 10966057 1 20140930 20140930 0