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
126859401 12685940 1 I 201601 20160121 20160825 20160825 PER US-FRI-1000082336 FOREST 74.00 YR M Y 87.54000 KG 20160825 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
126859401 12685940 1 PS LEXAPRO ESCITALOPRAM OXALATE 1 Oral 21323 10 MG TABLET
126859401 12685940 2 C LIPITOR ATORVASTATIN CALCIUM 1 Oral 40MG 0 40 MG QD
126859401 12685940 3 C ASA ASPIRIN 1 Oral 81MG 0 81 MG QD
126859401 12685940 4 C DYMISTA AZELASTINE HYDROCHLORIDEFLUTICASONE PROPIONATE 1 0
126859401 12685940 5 C POTASSIUM CITRATE. POTASSIUM CITRATE 1 Oral 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126859401 12685940 1 Depression
126859401 12685940 2 Blood cholesterol increased
126859401 12685940 3 Antiplatelet therapy
126859401 12685940 5 Renal lithiasis prophylaxis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126859401 12685940 Abdominal discomfort
126859401 12685940 Anxiety
126859401 12685940 Dizziness
126859401 12685940 Flatulence
126859401 12685940 Nausea
126859401 12685940 Somnolence
126859401 12685940 Thinking abnormal

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
126859401 12685940 1 20160119 0