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
126748813 12674881 3 F 20150417 20160912 20160823 20160919 EXP DE-ASTRAZENECA-2016SE88142 ASTRAZENECA 40.00 YR F Y 0.00000 20160919 OT NO NO

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
126748813 12674881 1 PS OMEPRAZOLE. OMEPRAZOLE 1 Oral 20 TO 40 MG, DAILY Y U 19810
126748813 12674881 2 C ATORVASTATIN ATORVASTATIN 1 0 20 MG QD
126748813 12674881 3 C ATORVASTATIN ATORVASTATIN 1 0 20 MG QD
126748813 12674881 4 C CERAZETTE DESOGESTREL 1 0 75 UG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126748813 12674881 1 Product used for unknown indication
126748813 12674881 2 Hypercholesterolaemia
126748813 12674881 3 Euphoric mood
126748813 12674881 4 Contraception

Outcome of event

Event ID CASEID OUTC COD
126748813 12674881 LT
126748813 12674881 HO
126748813 12674881 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126748813 12674881 Acute kidney injury
126748813 12674881 Cardiac arrest
126748813 12674881 Dehydration
126748813 12674881 Diarrhoea
126748813 12674881 Fatigue
126748813 12674881 Hypomagnesaemia
126748813 12674881 Loss of consciousness
126748813 12674881 Nausea
126748813 12674881 Palpitations
126748813 12674881 Stress
126748813 12674881 Torsade de pointes
126748813 12674881 Ventricular arrhythmia

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

no results found

Therapies reported

no results found