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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 8016617 | 8317508 | I | 8016617-1 | 20110926 | 20111223 | 20111231 | EXP | CHPA2011GB018718 | NOVARTIS CONSUMER HEALTH, INC. | 0 | YR | Y | 3.43 | KG | 20111231 | CN | UNITED KINGDOM |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 8016617 | 1018419886 | PS | FERROUS SULFATE TAB | 1 | TRANSPLACENTAL | UNK, UNK | |||||
| 8016617 | 1018419887 | SS | TYPHIM VI | 1 | TRANSPLACENTAL | 1 DF, ONCE/SINGLE | G0069 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 8016617 | 1018419887 | IMMUNISATION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 8016617 | CA |
Reactions reported
| Event ID | PT |
|---|---|
| 8016617 | FOETAL EXPOSURE DURING PREGNANCY |
| 8016617 | SYNDACTYLY |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 8016617 | 1018419886 | 20110515 | |||
| 8016617 | 1018419887 | 20110415 | 20110415 | 1 | DAY |