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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125738791 | 12573879 | 1 | I | 20160420 | 20160427 | 20160718 | 20160718 | PER | DL2016-0229 | DANCO | 28.00 | YR | F | N | 0.00000 | 20160629 | N | OT | US |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125738791 | 12573879 | 1 | PS | MIFEPRISTONE TABLETS, 200 MG (DANCO LABS) | MIFEPRISTONE | 1 | Oral | D | D | 13013001542 | 20181031 | 20687 | 200 | MG | |||||
| 125738791 | 12573879 | 2 | SS | MISOPROSTOL TABLETS, 200 MCG | MISOPROSTOL | 1 | Buccal | D | D | 0 | 800 | UG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125738791 | 12573879 | 1 | Abortion induced |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125738791 | 12573879 | Anaemia | |
| 125738791 | 12573879 | Asthenia | |
| 125738791 | 12573879 | Dizziness | |
| 125738791 | 12573879 | Haemorrhage | |
| 125738791 | 12573879 | Syncope |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | CASEID | RPSR COD |
|---|---|---|
| 125738791 | 12573879 | HP |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 125738791 | 12573879 | 1 | 20160407 | 0 | ||
| 125738791 | 12573879 | 2 | 20160408 | 0 |