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
126997202 12699720 2 F 201509 20160927 20160830 20160930 EXP US-ABBVIE-16P-163-1714462-00 ABBVIE 45.24 YR F Y 0.00000 20160930 CN COUNTRY NOT SPECIFIED 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
126997202 12699720 1 PS LUPRON DEPOT LEUPROLIDE ACETATE 1 Intramuscular Y UNKNOWN 19943 3.75 MG SUSPENSION FOR INJECTION /month
126997202 12699720 2 SS LUPRON DEPOT LEUPROLIDE ACETATE 1 Intramuscular D UNKNOWN,UNKNOWN 20708 11.25 MG SUSPENSION FOR INJECTION /month

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126997202 12699720 1 Uterine leiomyoma
126997202 12699720 2 Uterine leiomyoma

Outcome of event

Event ID CASEID OUTC COD
126997202 12699720 OT
126997202 12699720 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126997202 12699720 Haemorrhage
126997202 12699720 Muscle spasms
126997202 12699720 Pyrexia
126997202 12699720 Renal disorder
126997202 12699720 Sepsis
126997202 12699720 Urinary tract infection
126997202 12699720 Vaginal haemorrhage

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
126997202 12699720 1 201508 201510 0
126997202 12699720 2 20160812 0