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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126180971 | 12618097 | 1 | I | 20160718 | 20160803 | 20160803 | PER | US-JNJFOC-20160715344 | JANSSEN | 79.00 | YR | E | F | Y | 58.97000 | KG | 20160803 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126180971 | 12618097 | 1 | PS | ZYRTEC | CETIRIZINE HYDROCHLORIDE | 1 | Oral | 10 MG, 1 TABLET PER DAY, EVERY MORNING | N | 19835 | 10 | MG | TABLET | QD | |||||
126180971 | 12618097 | 2 | SS | ZYRTEC | CETIRIZINE HYDROCHLORIDE | 1 | Oral | 10 MG, 1 TABLET PER DAY, EVERY MORNING | N | 19835 | 10 | MG | TABLET | QD | |||||
126180971 | 12618097 | 3 | C | LISINOPRIL. | LISINOPRIL | 1 | Unknown | YEARS | 0 | 2.5 | MG | UNSPECIFIED | QD | ||||||
126180971 | 12618097 | 4 | C | SIMVASTATIN. | SIMVASTATIN | 1 | Unknown | YEARS | 0 | 10 | MG | UNSPECIFIED | QD | ||||||
126180971 | 12618097 | 5 | C | BABY ASPIRIN | ASPIRIN | 1 | Unknown | YEARS | 0 | 81 | MG | UNSPECIFIED | QD | ||||||
126180971 | 12618097 | 6 | C | VITAMIN D | CHOLECALCIFEROL | 1 | Unknown | YEARS | 0 | UNSPECIFIED |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126180971 | 12618097 | 1 | Rhinorrhoea |
126180971 | 12618097 | 2 | Multiple allergies |
126180971 | 12618097 | 3 | Hypertension |
126180971 | 12618097 | 4 | Blood cholesterol increased |
126180971 | 12618097 | 5 | Nutritional supplementation |
126180971 | 12618097 | 6 | Nutritional supplementation |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126180971 | 12618097 | Drug administration error |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |