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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126769171 | 12676917 | 1 | I | 201603 | 20160318 | 20160823 | 20160823 | PER | US-TEVA-645737USA | TEVA | 64.00 | YR | M | Y | 86.26000 | KG | 20160823 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126769171 | 12676917 | 1 | PS | CLONIDINE. | CLONIDINE | 1 | Transdermal | .1 MILLIGRAM DAILY; | 35984 | 79090 | .1 | MG | TRANSDERMAL PATCH | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126769171 | 12676917 | 1 | Blood pressure measurement |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126769171 | 12676917 | Application site erythema | |
126769171 | 12676917 | Application site irritation | |
126769171 | 12676917 | Application site urticaria |
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 |
---|---|---|---|---|---|---|
126769171 | 12676917 | 1 | 201602 | 201603 | 0 |