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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125947081 | 12594708 | 1 | I | 20160708 | 20160718 | 20160726 | 20160726 | EXP | GB-MHRA-TPP15336494C3318782YC1467987252411 | GB-DRREDDYS-GER/UKI/16/0081630 | DR REDDYS | 57.00 | YR | F | Y | 78.00000 | KG | 20160726 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125947081 | 12594708 | 1 | PS | AMLODIPINE | AMLODIPINE BESYLATE | 1 | U | U | UNKNOWN | 76692 | |||||||||
| 125947081 | 12594708 | 2 | C | RAMIPRIL. | RAMIPRIL | 1 | 1 | DF | 0 | 1 | DF | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125947081 | 12594708 | 1 | Product used for unknown indication |
| 125947081 | 12594708 | 2 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125947081 | 12594708 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125947081 | 12594708 | Gingival swelling | |
| 125947081 | 12594708 | Joint swelling |
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 |
|---|---|---|---|---|---|---|
| 125947081 | 12594708 | 1 | 20160318 | 0 | ||
| 125947081 | 12594708 | 2 | 20160708 | 0 |