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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126979851 | 12697985 | 1 | I | 20160810 | 20160822 | 20160830 | 20160830 | EXP | GB-MHRA-EYC 00143890 | GB-DRREDDYS-GER/UKI/16/0082672 | DR REDDYS | 43.00 | YR | F | Y | 110.67000 | KG | 20160830 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126979851 | 12697985 | 1 | PS | FLUOXETINE | FLUOXETINE HYDROCHLORIDE | 1 | U | U | UNKNOWN | 75465 | |||||||||
| 126979851 | 12697985 | 2 | I | DAKTARIN | MICONAZOLE NITRATE | 1 | Oral | 10 | ML | Y | U | GAB0Y00 | 0 | 2.5 | ML | GEL | QID | ||
| 126979851 | 12697985 | 3 | I | LORATADINE. | LORATADINE | 1 | U | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126979851 | 12697985 | 1 | Anxiety |
| 126979851 | 12697985 | 2 | Oral candidiasis |
| 126979851 | 12697985 | 3 | Seasonal allergy |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126979851 | 12697985 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126979851 | 12697985 | Diarrhoea | |
| 126979851 | 12697985 | Drug interaction |
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 |
|---|---|---|---|---|---|---|
| 126979851 | 12697985 | 2 | 20160810 | 20160811 | 0 |