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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127782791 | 12778279 | 1 | I | 20160916 | 20160920 | 20160926 | 20160926 | PER | US-JNJFOC-20160921846 | JOHNSON AND JOHNSON | 91.00 | YR | E | F | Y | 58.06000 | KG | 20160926 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127782791 | 12778279 | 1 | SS | ZYRTEC | CETIRIZINE HYDROCHLORIDE | 1 | Oral | U | 0 | 10 | MG | TABLET | |||||||
| 127782791 | 12778279 | 2 | SS | ZYRTEC | CETIRIZINE HYDROCHLORIDE | 1 | Oral | U | 0 | 10 | MG | TABLET | |||||||
| 127782791 | 12778279 | 3 | SS | ZYRTEC | CETIRIZINE HYDROCHLORIDE | 1 | Oral | U | 0 | 10 | MG | TABLET | |||||||
| 127782791 | 12778279 | 4 | PS | ZYRTEC | CETIRIZINE HYDROCHLORIDE | 1 | Oral | U | 19835 | 10 | MG | TABLET | |||||||
| 127782791 | 12778279 | 5 | SS | ZYRTEC | CETIRIZINE HYDROCHLORIDE | 1 | Oral | U | 19835 | 10 | MG | TABLET | |||||||
| 127782791 | 12778279 | 6 | C | AMLODIPINE | AMLODIPINE BESYLATE | 1 | Unknown | FOR YEARS | D | 0 | 5 | MG | UNSPECIFIED | ||||||
| 127782791 | 12778279 | 7 | C | ENALAPRIL | ENALAPRIL | 1 | Unknown | FOR YEARS | D | 0 | 10 | MG | UNSPECIFIED | ||||||
| 127782791 | 12778279 | 8 | C | PROMETHAZINE WITH CODEINE | CODEINE PHOSPHATEPROMETHAZINE HYDROCHLORIDE | 1 | Unknown | 1/2-1TSP 8 HOURS, FOR WEEK | D | 0 | SYRUP |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127782791 | 12778279 | 1 | Throat irritation |
| 127782791 | 12778279 | 2 | Lacrimation increased |
| 127782791 | 12778279 | 3 | Eye pruritus |
| 127782791 | 12778279 | 4 | Cough |
| 127782791 | 12778279 | 5 | Nasal congestion |
| 127782791 | 12778279 | 6 | Hypertension |
| 127782791 | 12778279 | 7 | Hypertension |
| 127782791 | 12778279 | 8 | Cough |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127782791 | 12778279 | Dizziness | |
| 127782791 | 12778279 | Drug administration error | |
| 127782791 | 12778279 | Drug ineffective for unapproved indication |
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 |
|---|---|---|---|---|---|---|
| 127782791 | 12778279 | 1 | 20160916 | 20160919 | 0 | |
| 127782791 | 12778279 | 2 | 20160916 | 20160919 | 0 | |
| 127782791 | 12778279 | 3 | 20160916 | 20160919 | 0 | |
| 127782791 | 12778279 | 4 | 20160916 | 20160919 | 0 | |
| 127782791 | 12778279 | 5 | 20160916 | 20160919 | 0 | |
| 127782791 | 12778279 | 8 | 20160918 | 0 |