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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125845451 | 12584545 | 1 | I | 19930811 | 20151030 | 20160722 | 20160722 | EXP | GB-MHRA-ADR 23212723 | GB-PFIZER INC-3082761 | PFIZER | 22.00 | YR | M | Y | 80.00000 | KG | 20160722 | OT | AU | AU |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125845451 | 12584545 | 1 | PS | PROPOFOL. | PROPOFOL | 1 | UNK | U | UNK | 77908 | EMULSION FOR INJECTION | ||||||||
| 125845451 | 12584545 | 2 | SS | PANADEINE FORTE | ACETAMINOPHENCODEINE PHOSPHATE | 1 | UNK | U | UNK | 0 | |||||||||
| 125845451 | 12584545 | 3 | SS | TORADOL | KETOROLAC TROMETHAMINE | 1 | Intramuscular | 30 MG,30 MG,QD, FREQ: 1 DAY; INTERVAL: 1 | UNK | 0 | 30 | MG | INJECTION | ||||||
| 125845451 | 12584545 | 4 | SS | TORADOL | KETOROLAC TROMETHAMINE | 1 | Intramuscular | 30 MG, CUMULATIVE DOSE: 60 MG, FREQ: 1 DAY; INTERVAL: 1 | UNK | 0 | 30 | MG | INJECTION | ||||||
| 125845451 | 12584545 | 5 | SS | FENTANYL CITRATE. | FENTANYL CITRATE | 1 | Unknown | UNK | U | UNK | 0 | ||||||||
| 125845451 | 12584545 | 6 | SS | OXYCODONE HYDROCHLORIDE. | OXYCODONE HYDROCHLORIDE | 1 | UNK | U | 0 | ||||||||||
| 125845451 | 12584545 | 7 | SS | VECURONIUM BROMIDE. | VECURONIUM BROMIDE | 1 | Unknown | UNK | U | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125845451 | 12584545 | 2 | General anaesthesia |
| 125845451 | 12584545 | 3 | General anaesthesia |
| 125845451 | 12584545 | 4 | Procedural pain |
| 125845451 | 12584545 | 5 | General anaesthesia |
| 125845451 | 12584545 | 6 | General anaesthesia |
| 125845451 | 12584545 | 7 | General anaesthesia |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125845451 | 12584545 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125845451 | 12584545 | Agitation | |
| 125845451 | 12584545 | Asthenia | |
| 125845451 | 12584545 | Back pain | |
| 125845451 | 12584545 | Blood creatine phosphokinase increased | |
| 125845451 | 12584545 | Blood creatinine increased | |
| 125845451 | 12584545 | Chills | |
| 125845451 | 12584545 | Chromaturia | |
| 125845451 | 12584545 | Muscular weakness | |
| 125845451 | 12584545 | Myalgia | |
| 125845451 | 12584545 | Nausea | |
| 125845451 | 12584545 | Off label use | |
| 125845451 | 12584545 | Product use issue | |
| 125845451 | 12584545 | Pyrexia | |
| 125845451 | 12584545 | Renal impairment | |
| 125845451 | 12584545 | Rhabdomyolysis | |
| 125845451 | 12584545 | Urine analysis abnormal | |
| 125845451 | 12584545 | Weight decreased |
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 |
|---|---|---|---|---|---|---|
| 125845451 | 12584545 | 3 | 19930809 | 19930809 | 0 | |
| 125845451 | 12584545 | 4 | 19930809 | 19930809 | 0 |