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
126249451 12624945 1 I 20160719 0 20160804 20160804 DIR 75.00 YR M N 0.00000 20160803 N OT 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
126249451 12624945 1 PS ADCIRCA TADALAFIL 1 Oral D D C521697A 20180901 0 40 MG QD
126249451 12624945 3 C LOSARTAN. LOSARTAN 1 0
126249451 12624945 5 C NASONEX MOMETASONE FUROATE 1 0
126249451 12624945 7 C FORADIL FORMOTEROL FUMARATE 1 0
126249451 12624945 9 C LIPITOR ATORVASTATIN CALCIUM 1 0
126249451 12624945 11 C OCUVITE VITAMINS 1 0
126249451 12624945 13 C SINGULAIR MONTELUKAST SODIUM 1 0
126249451 12624945 15 C ZYRTEC CETIRIZINE HYDROCHLORIDE 1 0
126249451 12624945 17 C PROBIOTIC PROBIOTICS NOS 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126249451 12624945 1 Pulmonary arterial hypertension

Outcome of event

Event ID CASEID OUTC COD
126249451 12624945 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
126249451 12624945 Death

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
126249451 12624945 1 20150130 20160719 0