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
90600171 9060017 1 I 20130117 0 20130207 20130207 DIR 78.00 YR M N 234.00000 LBS 20130125 CN 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
90600171 9060017 1 PS NIACOR 1 0
90600171 9060017 2 C ATENOLOL 1 0
90600171 9060017 3 C LISINOPRIL 1 0
90600171 9060017 4 C AMLODIPINE 1 0
90600171 9060017 6 C HYDROCHLOROTHIAZIDE 1 0
90600171 9060017 8 C CLOPIDOGREL 1 0
90600171 9060017 10 C PRASTATIN SODIUM 2 0
90600171 9060017 12 C LEVOTHYROXIN 1 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
90600171 9060017 RI

Reactions reported

Event ID CASEID DRUG REC ACT PT
90600171 9060017 Anxiety
90600171 9060017 Emotional distress
90600171 9060017 Erythema
90600171 9060017 Frustration
90600171 9060017 Insomnia
90600171 9060017 Pain
90600171 9060017 Pruritus
90600171 9060017 Skin burning sensation

Reporting Sources (this data is often not reported and may therefore be missing here)

Event ID CASEID RPSR COD
90600171 9060017 CSM

Therapies reported

no results found