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
125150343 12515034 3 F 20160628 20160630 20160706 EXP US-009507513-1606USA012164 MERCK 65.00 YR F Y 0.00000 20160706 OT 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
125150343 12515034 1 PS REMERON MIRTAZAPINE 1 Oral 15 MG, QD 20415 15 MG TABLET QD
125150343 12515034 2 C PHENOBARBITAL. PHENOBARBITAL 1 UNK U 0
125150343 12515034 3 C INDERAL PROPRANOLOL HYDROCHLORIDE 1 UNK U 0
125150343 12515034 4 C ADDERALL AMPHETAMINE ASPARTATEAMPHETAMINE SULFATEDEXTROAMPHETAMINE SACCHARATEDEXTROAMPHETAMINE SULFATE 1 Oral U 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125150343 12515034 1 Depression

Outcome of event

Event ID CASEID OUTC COD
125150343 12515034 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125150343 12515034 Abnormal dreams
125150343 12515034 Dyspnoea
125150343 12515034 Night sweats
125150343 12515034 Serotonin syndrome

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
125150343 12515034 1 20160625 0