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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125888151 | 12588815 | 1 | I | 20160525 | 20160602 | 20160725 | 20160725 | PER | US-JNJFOC-20160603566 | JANSSEN | 88.00 | YR | E | M | Y | 72.58000 | KG | 20160725 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125888151 | 12588815 | 1 | PS | ZYRTEC | CETIRIZINE HYDROCHLORIDE | 1 | Oral | N | 0242-136 | 19835 | TABLET | ||||||||
| 125888151 | 12588815 | 2 | SS | ZYRTEC | CETIRIZINE HYDROCHLORIDE | 1 | Oral | N | 0242-136 | 19835 | 10 | MG | TABLET | ||||||
| 125888151 | 12588815 | 3 | C | AMLODIPINE | AMLODIPINE BESYLATE | 1 | Unknown | 2 YEARS | 0 | 5 | MG | UNSPECIFIED | QD | ||||||
| 125888151 | 12588815 | 4 | C | CENTRUM SILVER | MINERALSVITAMINS | 1 | Unknown | 0 | UNSPECIFIED | ||||||||||
| 125888151 | 12588815 | 5 | C | VITAMIN B | VITAMIN B | 1 | Unknown | 0 | UNSPECIFIED | ||||||||||
| 125888151 | 12588815 | 6 | C | COQ10 | UBIDECARENONE | 1 | Unknown | 0 | UNSPECIFIED | ||||||||||
| 125888151 | 12588815 | 7 | C | THYROXINE | LEVOTHYROXINE | 1 | Unknown | 3 YEARS | 0 | 25 | MG | UNSPECIFIED | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125888151 | 12588815 | 2 | Rhinorrhoea |
| 125888151 | 12588815 | 3 | Hypertension |
| 125888151 | 12588815 | 4 | Product used for unknown indication |
| 125888151 | 12588815 | 5 | Product used for unknown indication |
| 125888151 | 12588815 | 6 | Product used for unknown indication |
| 125888151 | 12588815 | 7 | Hypothyroidism |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125888151 | 12588815 | Expired product administered | |
| 125888151 | 12588815 | Wrong patient received medication |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 125888151 | 12588815 | 2 | 20160525 | 0 |