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 |