Person who experienced the adverse event (patient)
| Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123169213 | 12316921 | 3 | F | 20160624 | 20160429 | 20160705 | EXP | US-JNJFOC-20160421361 | JOHNSON AND JOHNSON | 0.00 | F | Y | 0.00000 | 20160705 | CN | US | US |
Drug(s) used by person
| Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123169213 | 12316921 | 1 | PS | ZYRTEC | CETIRIZINE HYDROCHLORIDE | 1 | Oral | U | U | 474766 | 19835 | TABLET | |||||||
| 123169213 | 12316921 | 2 | SS | ZYRTEC | CETIRIZINE HYDROCHLORIDE | 1 | Oral | DOSAGE: HALF TABLET OF 10 MG DAILY (5MG) | U | U | 474766 | 19835 | TABLET | ||||||
| 123169213 | 12316921 | 3 | SS | ALLERGY MEDICATION | DIPHENHYDRAMINE HYDROCHLORIDE | 1 | Unknown | EVERY 2 WEEKS, YEARS | 0 | UNSPECIFIED | |||||||||
| 123169213 | 12316921 | 4 | C | HYDROCHLOROTHIAZIDE. | HYDROCHLOROTHIAZIDE | 1 | Unknown | 0 | 25 | MG | UNSPECIFIED | ||||||||
| 123169213 | 12316921 | 5 | C | HYDROLATUM | 2 | Unknown | 0 | CREAM | |||||||||||
| 123169213 | 12316921 | 6 | C | AMLODIPINE | AMLODIPINE BESYLATE | 1 | Unknown | 0 | 5 | MG | UNSPECIFIED | ||||||||
| 123169213 | 12316921 | 7 | C | SYNTHROID | LEVOTHYROXINE SODIUM | 1 | Unknown | 0 | UNSPECIFIED |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 123169213 | 12316921 | 2 | Multiple allergies |
| 123169213 | 12316921 | 3 | Multiple allergies |
| 123169213 | 12316921 | 4 | Product used for unknown indication |
| 123169213 | 12316921 | 5 | Product used for unknown indication |
| 123169213 | 12316921 | 6 | Product used for unknown indication |
| 123169213 | 12316921 | 7 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 123169213 | 12316921 | HO |
| 123169213 | 12316921 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 123169213 | 12316921 | Large intestine perforation | |
| 123169213 | 12316921 | Wrong patient received medication |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |