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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125796731 | 12579673 | 1 | I | 20160609 | 20160711 | 20160721 | 20160721 | EXP | GB-MHRA-EYC 00142055 | GB-TEVA-676880ACC | TEVA | 27.00 | YR | F | Y | 56.00000 | KG | 20160721 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125796731 | 12579673 | 1 | PS | TRIMETHOPRIM. | TRIMETHOPRIM | 1 | Oral | 2 DOSAGE FORMS DAILY; | 28 | DF | U | 18679 | 1 | DF | TABLET | BID | |||
| 125796731 | 12579673 | 2 | C | PREDNISOLONE. | PREDNISOLONE | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125796731 | 12579673 | 1 | Urinary tract infection |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125796731 | 12579673 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125796731 | 12579673 | Dysphagia | |
| 125796731 | 12579673 | Dyspnoea | |
| 125796731 | 12579673 | Oropharyngeal pain | |
| 125796731 | 12579673 | Pain | |
| 125796731 | 12579673 | Rash papular | |
| 125796731 | 12579673 | Throat tightness |
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 |
|---|---|---|---|---|---|---|
| 125796731 | 12579673 | 1 | 20160526 | 20160528 | 0 |