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
98933833 9893383 3 F 20120823 20140930 20140213 20141001 EXP US-009507513-1402USA005076 MERCK 0.00 F Y 61.68000 KG 20141001 N 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
98933833 9893383 1 PS NUVARING ETHINYL ESTRADIOLETONOGESTREL 1 VAGINAL 0.12 MG/0.015 MG/24 HR; LEAVE IN FOR 21 DAYS, REMOVE FOR 7 DAYS, THEN REPEAT CYCLE D 21187 1 DF VAGINAL RING /month
98933833 9893383 2 C VITAMINS (UNSPECIFIED) VITAMINS 1 ORAL U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
98933833 9893383 1 Product used for unknown indication
98933833 9893383 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
98933833 9893383 HO
98933833 9893383 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
98933833 9893383 Breast prosthesis implantation
98933833 9893383 Hyperpituitarism
98933833 9893383 Menstruation delayed
98933833 9893383 Nephrolithiasis
98933833 9893383 Pituitary tumour
98933833 9893383 Pulmonary embolism

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

no results found

Therapies reported

no results found