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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6810138 | 7357486 | F | 6810138-7 | 20100101 | 20100622 | 20100630 | EXP | US-JNJCH-2010008851 | JNJCH | 2 | YR | M | Y | 16.3 | KG | 20100630 | CN | UNITED STATES |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6810138 | 1014006352 | PS | CHILDREN'S ZYRTEC ALLERGY | 1 | ORAL | TEXT:1/2 TSP PRN | AFM302 | 022155 | |||
| 6810138 | 1014006353 | C | NEXIUM | 1 | UNKNOWN | TEXT:UNKNOWN |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6810138 | 1014006352 | SEASONAL ALLERGY |
| 6810138 | 1014006353 | GASTROOESOPHAGEAL REFLUX DISEASE |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6810138 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 6810138 | AGGRESSION |
| 6810138 | DECREASED APPETITE |
| 6810138 | DEHYDRATION |
| 6810138 | DIARRHOEA HAEMORRHAGIC |
| 6810138 | GASTRITIS |
| 6810138 | GASTROOESOPHAGEAL REFLUX DISEASE |
| 6810138 | MUCOUS STOOLS |
| 6810138 | PRODUCT QUALITY ISSUE |
| 6810138 | SOMNOLENCE |
| 6810138 | VIRAL INFECTION |
| 6810138 | WEIGHT DECREASED |
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 |
|---|---|---|---|---|---|
| 6810138 | 1014006352 | 20100101 | 20100411 |