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
125308061 12530806 1 I 0 20160705 20160705 DIR 72.00 YR M N 183.00000 LBS 20160701 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
125308061 12530806 1 PS ATORVASTATIN (LAST STATIN TAKEN), 40 MG ATORVASTATIN 1 Oral N D L03 0 1 DF COATED TABLET HS
125308061 12530806 2 SS SIMVASTATIN. SIMVASTATIN 1 0
125308061 12530806 4 C GABAPENTIN. GABAPENTIN 1 0
125308061 12530806 6 C ACETAMINOPHENHYDROCODONE BITARTRATE ACETAMINOPHENHYDROCODONE BITARTRATE 1 0
125308061 12530806 8 C MULTIVITAMIN VITAMINS 1 0
125308061 12530806 10 C COQ10 UBIDECARENONE 1 0
125308061 12530806 12 C VITAMIN D3 CHOLECALCIFEROL 1 0
125308061 12530806 14 C MAGNESIUM MAGNESIUM 1 0
125308061 12530806 16 C ASPIRIN. ASPIRIN 1 0
125308061 12530806 18 C OMEGA 3 OMEGA-3 FATTY ACIDS 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125308061 12530806 1 Stent placement

Outcome of event

Event ID CASEID OUTC COD
125308061 12530806 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125308061 12530806 Arthralgia
125308061 12530806 Decreased activity
125308061 12530806 Hypoaesthesia
125308061 12530806 Muscle atrophy
125308061 12530806 Myalgia

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
125308061 12530806 1 5 YR