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
127058231 12705823 1 I 20151207 0 20160831 20160831 DIR 74.00 YR F N 144.00000 LBS 20160818 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
127058231 12705823 1 PS MULTAQ DRONEDARONE 1 Oral N D 20161203 0 1 DF COATED TABLET BID
127058231 12705823 3 C LIPITOR ATORVASTATIN CALCIUM 1 0
127058231 12705823 5 C DILTIAZEM. DILTIAZEM 1 0
127058231 12705823 7 C EPIE PEN 2 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127058231 12705823 1 Palpitations
127058231 12705823 1 Supraventricular extrasystoles

Outcome of event

Event ID CASEID OUTC COD
127058231 12705823 HO
127058231 12705823 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127058231 12705823 Acute kidney injury
127058231 12705823 Dehydration
127058231 12705823 Hypokalaemia
127058231 12705823 Hyponatraemia
127058231 12705823 Leukocytosis
127058231 12705823 Thrombocytosis
127058231 12705823 Tubulointerstitial nephritis
127058231 12705823 Weight decreased

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
127058231 12705823 1 20151204 20151227 0