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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126819072 | 12681907 | 2 | F | 20150713 | 20160914 | 20160824 | 20160923 | EXP | GB-MHRA-EYC 00143754 | GB-MYLANLABS-2016M1034739 | MYLAN | 0.00 | Y | 0.00000 | 20160923 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126819072 | 12681907 | 1 | PS | AMLODIPINE | AMLODIPINE BESYLATE | 1 | Oral | 10 MG, UNK | Y | U | 76418 | 10 | MG | ||||||
| 126819072 | 12681907 | 2 | C | PERINDOPRIL ARGININE | PERINDOPRIL ARGININE | 1 | UNK | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126819072 | 12681907 | 1 | Hypertension |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126819072 | 12681907 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126819072 | 12681907 | Arthralgia | |
| 126819072 | 12681907 | Joint swelling | |
| 126819072 | 12681907 | Muscle spasms | |
| 126819072 | 12681907 | Musculoskeletal stiffness | |
| 126819072 | 12681907 | Peripheral swelling | |
| 126819072 | 12681907 | Trigger finger |
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 |
|---|---|---|---|---|---|---|
| 126819072 | 12681907 | 1 | 20150622 | 20160712 | 0 |