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
120808614 12080861 4 F 201502 20160808 20160216 20160812 PER US-BAYER-2016-029653 BAYER 27.00 YR A F Y 52.15000 KG 20160812 CN US 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
120808614 12080861 1 PS MIRENA LEVONORGESTREL 1 Intra-uterine 20 MCG/24HR, CONT TU00X6D 21225 20 UG INTRAUTERINE DELIVERY SYSTEM
120808614 12080861 2 C TYLENOL WITH CODEIN [CAFFEINE,CODEINE PHOSPHATE,PARACETAMOL] 2 0
120808614 12080861 3 C KEFLEX CEPHALEXIN 1 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
120808614 12080861 OT
120808614 12080861 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
120808614 12080861 Abdominal pain
120808614 12080861 Abdominal pain lower
120808614 12080861 Anxiety
120808614 12080861 Depression
120808614 12080861 Device issue
120808614 12080861 Fear of disease
120808614 12080861 Post procedural haemorrhage
120808614 12080861 Procedural pain
120808614 12080861 Sexual aversion disorder
120808614 12080861 Stress
120808614 12080861 Uterine perforation

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
120808614 12080861 1 20150203 20150727 0