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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 103817321 | 10381732 | 1 | I | 20140422 | 20140806 | 20140813 | 20140813 | EXP | GB-MHRA-EYC 00113475 | GB-TEVA-500125ISR | TEVA | 68.00 | YR | M | Y | 0.00000 | 20140813 | N | PH | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 103817321 | 10381732 | 1 | PS | NITROFURANTOIN. | NITROFURANTOIN | 1 | ORAL | 50 MILLIGRAM DAILY; | 50 | MG | U | NOT KNOWN | 73652 | 50 | MG | QD | |||
| 103817321 | 10381732 | 2 | C | PARACETAMOL | ACETAMINOPHEN | 1 | D | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 103817321 | 10381732 | 1 | Cystitis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 103817321 | 10381732 | DS |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 103817321 | 10381732 | Hallucination | |
| 103817321 | 10381732 | Nightmare |
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 |
|---|---|---|---|---|---|---|
| 103817321 | 10381732 | 1 | 20140422 | 20140423 | 0 |