The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
8625026 8190065 F 8625026-3 20110301 20120814 20120827 EXP PT-009507513-2011SP045901 MERCK AND CO INC YR Y 20120827 OT UNITED STATES

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
8625026 1020676086 I GARDASIL 2 INTRAMUSCULAR 1 DF
8625026 1020676087 I GARDASIL 2 INTRAMUSCULAR 1 DF
8625026 1020676085 PS IMPLANON 1 SUBCUTANEOUS 1 DF, UNK 21529
8625026 1020676088 I GARDASIL 2 INTRAMUSCULAR 1 DF
8625026 1020676089 I MINIGESTE 2 ORAL 1 DF, QD

Indications of drugs used

Event ID DRUG SEQ INDI PT
8625026 1020676085 CONTRACEPTION
8625026 1020676089 MENORRHAGIA

Outcome of event

Event ID OUTC COD
8625026 OT
8625026 HO

Reactions reported

Event ID PT
8625026 CEREBRAL VENOUS THROMBOSIS
8625026 MEDICATION ERROR
8625026 DRUG INTERACTION
8625026 GRAND MAL CONVULSION

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

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
8625026 1020676086 20110119 20110119 1 DAY
8625026 1020676087 20110404 20110404 1 DAY
8625026 1020676085 20110301 20110901
8625026 1020676088 20110901 20110901 1 DAY
8625026 1020676089 20090101 20110817