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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125739141 | 12573914 | 1 | I | 20150729 | 20160411 | 20160718 | 20160718 | PER | DL2016-0200 | DANCO | 27.00 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125739141 | 12573914 | 1 | PS | MIFEPRISTONE TABLETS, 200 MG (DANCO LABS) | MIFEPRISTONE | 1 | Oral | D | D | 13001002270 | 20180228 | 20687 | 200 | MG | |||||
125739141 | 12573914 | 2 | SS | MISOPROSTOL TABLETS, 200 MCG | MISOPROSTOL | 1 | Buccal | D | D | 0 | 800 | UG | |||||||
125739141 | 12573914 | 4 | C | METRONIDAZOLE. | METRONIDAZOLE | 1 | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125739141 | 12573914 | 1 | Abortion induced |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125739141 | 12573914 | Abortion incomplete | |
125739141 | 12573914 | Haemorrhage | |
125739141 | 12573914 | Headache |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | CASEID | RPSR COD |
---|---|---|
125739141 | 12573914 | HP |
Therapies reported
Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|---|
125739141 | 12573914 | 1 | 20150721 | 0 | ||
125739141 | 12573914 | 2 | 20150722 | 0 | ||
125739141 | 12573914 | 2 | 20150804 | 0 |