Person who experienced the adverse event (patient)
Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5957530 | 6996336 | I | 5957530-0 | 20081028 | 20081112 | EXP | B0545198A | GLAXOSMITHKLINE | F | N | 20081110 | MD | INDIA |
Drug(s) used by person
Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
---|---|---|---|---|---|---|---|---|---|---|---|
5957530 | 1010720251 | PS | PROPRANOLOL HYDROCHLORIDE | 1 | TRANSPLACENTAL | 30 MG, PER DAY, TRANSPLACENTARY | Y | D | 21438 | ||
5957530 | 1010738808 | SS | CARBIMAZOLE | 2 | TRANSPLACENTAL | 40 MG, PER DAY, TRANSPLACENTARY | D | D | |||
5957530 | 1010738824 | SS | METHYLDOPA | 1 | TRANSPLACENTAL | TRANSPLACENTARY | D | D |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
5957530 | CA |
5957530 | RI |
Reactions reported
Event ID | PT |
---|---|
5957530 | CAESAREAN SECTION |
5957530 | CHOANAL ATRESIA |
5957530 | CYANOSIS |
5957530 | MATERNAL DRUGS AFFECTING FOETUS |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
5957530 | FGN |
5957530 | HP |
5957530 | LIT |
Therapies reported
Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|
5957530 | 1010738824 | 2 | WK |