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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127198261 | 12719826 | 1 | I | 20150928 | 20160907 | 20160907 | PER | US-AUROBINDO-AUR-APL-2015-08918 | AUROBINDO | 0.00 | F | Y | 0.00000 | 20160907 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127198261 | 12719826 | 1 | PS | HYDROCHLOROTHIAZIDE. | HYDROCHLOROTHIAZIDE | 1 | Unknown | UNK | U | U | 40780 | ||||||||
127198261 | 12719826 | 2 | SS | LISINOPRIL. | LISINOPRIL | 1 | Unknown | UNK | U | U | 0 | ||||||||
127198261 | 12719826 | 3 | SS | LEVOXYL | LEVOTHYROXINE SODIUM | 1 | Unknown | U | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127198261 | 12719826 | 1 | Hypertension |
127198261 | 12719826 | 2 | Hypertension |
127198261 | 12719826 | 3 | Product used for unknown indication |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127198261 | 12719826 | Chest discomfort | |
127198261 | 12719826 | Flushing | |
127198261 | 12719826 | Headache | |
127198261 | 12719826 | Heart rate increased |
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 |
---|---|---|---|---|---|---|
127198261 | 12719826 | 1 | 201503 | 0 | ||
127198261 | 12719826 | 2 | 201503 | 0 |