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
4628736 4056259 F 1 4628736-8 20030101 20050323 20050406 EXP 03-000513 WARNER CHILCOTT F N 20050401 MD 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
4628736 1005852887 PS FEMHRT 1 ORAL 5/1000 UG QD, ORAL U U 21065

Indications of drugs used

Event ID DRUG SEQ INDI PT
4628736 1005852887 NIGHT SWEATS

Outcome of event

Event ID OUTC COD
4628736 HO

Reactions reported

Event ID PT
4628736 CONDITION AGGRAVATED
4628736 DIFFICULTY IN WALKING
4628736 FIBROMYALGIA
4628736 HYPOAESTHESIA
4628736 MUSCLE SPASMS
4628736 OEDEMA PERIPHERAL
4628736 RASH MACULAR

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

Event ID RPSR COD
4628736 HP

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
4628736 1005852887 20031001