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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125883351 | 12588335 | 1 | I | 20160516 | 20160725 | 20160725 | PER | US-JNJFOC-20160516072 | JANSSEN | 70.00 | YR | E | M | Y | 68.04000 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125883351 | 12588335 | 1 | PS | ZYRTEC | CETIRIZINE HYDROCHLORIDE | 1 | Oral | (1/2 TABLET IN THE MORNING AND 1/2 IN THE EVENING); IN THE PAST 3-4 DAYS | N | Y | 471353 | 19835 | .5 | DF | TABLET | BID | |||
| 125883351 | 12588335 | 2 | SS | ZYRTEC | CETIRIZINE HYDROCHLORIDE | 1 | Oral | IN THE PAST 6-12 MONTHS | N | Y | 471353 | 19835 | 1.5 | DF | TABLET | QD | |||
| 125883351 | 12588335 | 3 | SS | IBUPROFEN. | IBUPROFEN | 1 | Unknown | 1 YEAR | U | 0 | 200 | MG | UNSPECIFIED | BID | |||||
| 125883351 | 12588335 | 4 | C | FLONASE | FLUTICASONE PROPIONATE | 1 | Unknown | 0 | 2 | DF | SPRAY | BID | |||||||
| 125883351 | 12588335 | 5 | C | VENTOLINE | ALBUTEROL | 1 | Unknown | 2 DAYS | 0 | 2 | DF | INHALATION |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125883351 | 12588335 | 1 | Multiple allergies |
| 125883351 | 12588335 | 2 | Multiple allergies |
| 125883351 | 12588335 | 3 | Pain management |
| 125883351 | 12588335 | 4 | Nasal inflammation |
| 125883351 | 12588335 | 5 | Chronic obstructive pulmonary disease |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125883351 | 12588335 | Chest discomfort | Chest discomfort |
| 125883351 | 12588335 | Dizziness | Dizziness |
| 125883351 | 12588335 | Hypoaesthesia | Hypoaesthesia |
| 125883351 | 12588335 | Prescribed overdose | |
| 125883351 | 12588335 | Rash | Rash |
| 125883351 | 12588335 | Throat tightness | Throat tightness |
| 125883351 | 12588335 | Tinnitus | Tinnitus |
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 |
|---|---|---|---|---|---|---|
| 125883351 | 12588335 | 1 | 20160516 | 0 | ||
| 125883351 | 12588335 | 5 | 20160514 | 0 |