The Safety Rates Drug Report

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Drug     Injury     Quarter    

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
126124801 12612480 1 I 201508 20150827 20160801 20160801 PER US-PRINSTON PHARMACEUTICAL INC.-2015RIS00131 PRINSTON PHARMACEUTICAL 61.04 YR F Y 76.64000 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
126124801 12612480 1 PS LOSARTAN POTASSIUM. LOSARTAN POTASSIUM 1 Oral 100 MG, 1X/DAY UNK 91497 100 MG TABLET QD
126124801 12612480 2 C PRAVASTATIN. PRAVASTATIN 1 UNK 0
126124801 12612480 3 C NEXIUM ESOMEPRAZOLE MAGNESIUM 1 UP TO 40 MG/D 0
126124801 12612480 4 C ZOLOFT SERTRALINE HYDROCHLORIDE 1 25 MG, UNK 0 25 MG
126124801 12612480 5 C XANAX ALPRAZOLAM 1 UNK, AS NEEDED 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126124801 12612480 1 Hypertension

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126124801 12612480 Abdominal pain upper
126124801 12612480 Blood pressure increased
126124801 12612480 Decreased appetite
126124801 12612480 Drug ineffective
126124801 12612480 Head discomfort
126124801 12612480 Headache
126124801 12612480 Malaise
126124801 12612480 Nausea
126124801 12612480 Palpitations
126124801 12612480 Product substitution issue

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
126124801 12612480 1 201508 0