The Safety Rates Drug Report

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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
126124871 12612487 1 I 201604 20160418 20160801 20160801 PER US-PRINSTON PHARMACEUTICAL INC.-2016RIS00048 PRINSTON PHARMACEUTICAL 74.61 YR F Y 88.89000 KG 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
126124871 12612487 1 PS LOSARTAN POTASSIUM. LOSARTAN POTASSIUM 1 Oral 100 MG, 1X/DAY 91497 100 MG TABLET QD
126124871 12612487 2 C HYDROCODONE 10/325 ACETAMINOPHENHYDROCODONE BITARTRATE 1 0
126124871 12612487 3 C CLONIDINE. CLONIDINE 1 0.2 MG, 1X/DAY 0 .2 MG QD
126124871 12612487 4 C CLONIDINE. CLONIDINE 1 0.1 MG, 1X/DAY 0 .1 MG QD
126124871 12612487 5 C METOPROLOL. METOPROLOL 1 12.5 MG, 2X/DAY 0 12.5 MG BID
126124871 12612487 6 C BABY ASPIRIN ASPIRIN 1 UNK UNK, 1X/DAY 0 QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126124871 12612487 1 Hypertension

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126124871 12612487 Diarrhoea
126124871 12612487 Discomfort
126124871 12612487 Nausea

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
126124871 12612487 1 20160411 0