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
125920291 12592029 1 I 20160706 0 20160725 20160725 DIR 69.00 YR F N 162.00000 LBS 20160723 N 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
125920291 12592029 1 PS METOPROLOL. METOPROLOL 1 Oral Y D LL 92-5 20170613 0 270 DF COATED TABLET BID
125920291 12592029 3 C VISITOR 2 0
125920291 12592029 5 C SINGULAIR MONTELUKAST SODIUM 1 0
125920291 12592029 7 C SYMBOLOGY 2 0
125920291 12592029 9 C MANASSAS 2 0
125920291 12592029 11 C FIORACET ACETAMINOPHENBUTALBITALCAFFEINE 1 0
125920291 12592029 13 C VITAMIN D CHOLECALCIFEROL 1 0
125920291 12592029 15 C MULTIVITAMINS VITAMINS 1 0
125920291 12592029 17 C CHLORTRIMETON CHLORPHENIRAMINE MALEATE 1 0
125920291 12592029 19 C PHILLIPS MILK OF MAGNESIA 2 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125920291 12592029 1 Hypertension

Outcome of event

Event ID CASEID OUTC COD
125920291 12592029 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125920291 12592029 Blood pressure decreased
125920291 12592029 Blood pressure increased
125920291 12592029 Dizziness
125920291 12592029 Drug ineffective
125920291 12592029 Fatigue
125920291 12592029 Feeling abnormal
125920291 12592029 Headache
125920291 12592029 Malaise
125920291 12592029 Nausea
125920291 12592029 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
125920291 12592029 1 20160701 20160710 0