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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126124831 | 12612483 | 1 | I | 2015 | 20151016 | 20160801 | 20160801 | PER | US-PRINSTON PHARMACEUTICAL INC.-2015RIS00147 | PRINSTON PHARMACEUTICAL | 0.00 | M | Y | 0.00000 | 20160705 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126124831 | 12612483 | 1 | PS | LOSARTAN POTASSIUM. | LOSARTAN POTASSIUM | 1 | UNK | U | U | 91497 | TABLET | ||||||||
126124831 | 12612483 | 2 | SS | LOSARTAN (ZYDUS) | LOSARTAN | 1 | UNK | 0 |
Indications of drugs used
no results found |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126124831 | 12612483 | Blood pressure fluctuation | |
126124831 | 12612483 | Diarrhoea | |
126124831 | 12612483 | Drug ineffective | |
126124831 | 12612483 | Hypotonia | |
126124831 | 12612483 | Muscle injury | |
126124831 | 12612483 | Myalgia | |
126124831 | 12612483 | Prerenal failure |
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 |
---|---|---|---|---|---|---|
126124831 | 12612483 | 1 | 201502 | 0 | ||
126124831 | 12612483 | 2 | 201502 | 0 |