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
126127741 12612774 1 I 20160711 20160801 20160801 EXP BR-ELI_LILLY_AND_COMPANY-BR201607004862 ELI LILLY AND CO 0.00 F Y 48.00000 KG 20160801 CN BR BR

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
126127741 12612774 1 PS HUMULIN N INSULIN HUMAN 1 Subcutaneous 20 IU, EACH MORNING 18780 20 IU INJECTION QD
126127741 12612774 2 SS HUMULIN N INSULIN HUMAN 1 Subcutaneous UNK UNK, EACH EVENING 18780 INJECTION QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126127741 12612774 1 Diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
126127741 12612774 HO
126127741 12612774 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126127741 12612774 Amniorrhoea
126127741 12612774 Amniotic fluid index decreased
126127741 12612774 Diabetic metabolic decompensation
126127741 12612774 Maternal exposure during pregnancy
126127741 12612774 Placental disorder
126127741 12612774 Pre-eclampsia

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
126127741 12612774 1 2013 201409 0
126127741 12612774 2 2013 201409 0