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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 7205769 | 7745354 | I | 7205769-9 | 20100720 | 20101220 | 20101231 | EXP | CHPA2010FR13748 | NOVARTIS CONSUMER HEALTH, INC. | 35 | YR | F | Y | 20101230 | MD | FRANCE |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 7205769 | 1015450435 | PS | SCOPOLAMINE | 1 | TRANSDERMAL | 1 MG, Q72H PRN | 0830021 | 017874 | |||
| 7205769 | 1015450436 | C | DIFFU K | 2 | ORAL | 4 CAPSULES, QD |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 7205769 | 1015450435 | MOTION SICKNESS |
| 7205769 | 1015450436 | HYPOKALAEMIA |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 7205769 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 7205769 | CAESAREAN SECTION |
| 7205769 | DIPLOPIA |
| 7205769 | DRUG EXPOSURE DURING PREGNANCY |
| 7205769 | DRUG INEFFECTIVE |
| 7205769 | DRY MOUTH |
| 7205769 | NORMAL NEWBORN |
| 7205769 | PRE-ECLAMPSIA |
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 |
|---|---|---|---|---|---|
| 7205769 | 1015450435 | 20100716 | 20100717 | 2 | DAY |
| 7205769 | 1015450436 | 20080101 |