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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127075931 | 12707593 | 1 | I | 20160814 | 20160824 | 20160901 | 20160901 | EXP | GB-MHRA-EYC 00144050 | PHHY2016GB116671 | SANDOZ | 57.00 | YR | F | Y | 88.90000 | KG | 20160901 | OT | GB | GB |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127075931 | 12707593 | 1 | PS | TRAMADOL HYDROCHLORIDE. | TRAMADOL HYDROCHLORIDE | 1 | Oral | 50 MG, UNK | Y | U | 283410 | 75968 | 50 | MG | |||||
127075931 | 12707593 | 2 | C | PARACETAMOL | ACETAMINOPHEN | 1 | Unknown | 2 DF, UNK | U | 0 | 2 | DF |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127075931 | 12707593 | 1 | Sciatica |
127075931 | 12707593 | 2 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127075931 | 12707593 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127075931 | 12707593 | Disturbance in attention | |
127075931 | 12707593 | Dizziness | |
127075931 | 12707593 | Haematemesis | |
127075931 | 12707593 | Hyperhidrosis |
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 |
---|---|---|---|---|---|---|
127075931 | 12707593 | 1 | 20160814 | 20160815 | 0 | |
127075931 | 12707593 | 2 | 20160815 | 0 |