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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5722904 | 6581100 | F | 1 | 5722904-X | 20080203 | 20080417 | 20080425 | EXP | PHBS2008EC02093 | NOVARTIS CONSUMER HEALTH, INC. | 43 | YR | M | N | 20080424 | CN | ECUADOR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5722904 | 1009853673 | PS | CATAFLAM | 1 | ORAL | 2 TABLETS/DAY, ORAL | Y | U | |||
| 5722904 | 1009901150 | SS | ZURCAL(PANTOPRAZOLE) TABLET | 2 | ORAL | 40 MG, QD, ORAL | U | U | |||
| 5722904 | 1009901151 | SS | ACETAMINOPHEN (PARACETAMOL),CHLORPHENIRAM,DEXTROMETHORPHAN HBR (NCH)(P | 2 | ORAL | UP TO 6 TABLETS/DAY, ORAL | Y | U |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5722904 | 1009853673 | ARTHRALGIA |
| 5722904 | 1009901151 | PHARYNGITIS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5722904 | HO |
| 5722904 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5722904 | GASTRIC HAEMORRHAGE |
| 5722904 | GASTRITIS |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 5722904 | FGN |
| 5722904 | OTH |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 5722904 | 1009853673 | 20080119 | 20080201 | ||
| 5722904 | 1009901151 | 20080119 | 20080201 |