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
126248161 12624816 1 I 20160802 0 20160804 20160804 DIR 58.00 YR M N 160.00000 LBS 20160803 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
126248161 12624816 1 PS AMLODIPINE AMLODIPINE BESYLATE 1 Oral D 20171031 0 1 DF COATED TABLET HS
126248161 12624816 2 C FINASTERIDE. FINASTERIDE 1 0
126248161 12624816 3 C ATORVASTATIN ATORVASTATIN 1 0
126248161 12624816 4 C FLUTICASONE PROPIONATE. FLUTICASONE PROPIONATE 1 0
126248161 12624816 5 C ROGAINE SPRAY 2 0
126248161 12624816 6 C MULTIVITAMINS VITAMINS 1 0
126248161 12624816 7 C MAGNESIUM MAGNESIUM 1 0
126248161 12624816 8 C POTASSIUM POTASSIUM 1 0
126248161 12624816 9 C VITAMIN D3 CHOLECALCIFEROL 1 0
126248161 12624816 10 C BABY ASPIRIN ASPIRIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126248161 12624816 1 Hypertension

Outcome of event

Event ID CASEID OUTC COD
126248161 12624816 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126248161 12624816 Dermatitis
126248161 12624816 Dysgeusia
126248161 12624816 Lacrimation increased
126248161 12624816 Muscle fatigue
126248161 12624816 Peripheral swelling
126248161 12624816 Pruritus
126248161 12624816 Stomatitis
126248161 12624816 Thyroid disorder

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
126248161 12624816 1 20160627 20160803 0