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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124157763 | 12415776 | 3 | F | 20160622 | 20160530 | 20160707 | EXP | GB-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-117485 | RANBAXY | 0.00 | F | Y | 0.00000 | 20160707 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124157763 | 12415776 | 1 | PS | RISPERIDONE. | RISPERIDONE | 1 | Oral | DOSAGE FORM: UNSPECIFIED | U | U | UNKNOWN | 77542 | 3 | MG | |||||
| 124157763 | 12415776 | 2 | SS | XEPLION | PALIPERIDONE PALMITATE | 1 | Intramuscular | 150 MG, UNK | U | U | UNKNOWN | 0 | 150 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 124157763 | 12415776 | 1 | Product used for unknown indication |
| 124157763 | 12415776 | 2 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 124157763 | 12415776 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124157763 | 12415776 | Hospitalisation | |
| 124157763 | 12415776 | Malaise | |
| 124157763 | 12415776 | Treatment noncompliance |
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 |
|---|---|---|---|---|---|---|
| 124157763 | 12415776 | 2 | 201503 | 0 |