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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126968731 | 12696873 | 1 | I | 20160801 | 20160817 | 20160830 | 20160830 | EXP | GB-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-122568 | RANBAXY | 68.00 | YR | M | Y | 79.00000 | KG | 20160830 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126968731 | 12696873 | 1 | PS | VENLAFAXINE | VENLAFAXINE HYDROCHLORIDE | 1 | Oral | 37.5 MG, BID | 75 | MG | Y | U | 91272 | 37.5 | MG | Q12H | |||
| 126968731 | 12696873 | 2 | C | ACTAVIS UK DIAZEPAM | DIAZEPAM | 1 | Unknown | U | U | 0 | |||||||||
| 126968731 | 12696873 | 3 | C | ACTAVIS UK ZOPICLONE | ZOPICLONE | 1 | Unknown | U | U | 0 | |||||||||
| 126968731 | 12696873 | 4 | C | AMLODIPINE | AMLODIPINE BESYLATE | 1 | Unknown | U | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126968731 | 12696873 | 1 | Anxiety |
| 126968731 | 12696873 | 2 | Product used for unknown indication |
| 126968731 | 12696873 | 3 | Product used for unknown indication |
| 126968731 | 12696873 | 4 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126968731 | 12696873 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126968731 | 12696873 | Decreased appetite | |
| 126968731 | 12696873 | Depression | |
| 126968731 | 12696873 | Feeling abnormal | |
| 126968731 | 12696873 | Hyperhidrosis | |
| 126968731 | 12696873 | Sensory disturbance |
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 |
|---|---|---|---|---|---|---|
| 126968731 | 12696873 | 1 | 20160801 | 20160808 | 0 |