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
5195431 6206041 F 5195431-9 20030722 20060405 20061230 EXP US-NOVOPROD-252273 NOVOPROD F Y 86.168 KG 20061230 LW 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
5195431 1007999387 PS ACTIVELLA 1 1 MG/0.5 MG QD UNKNOWN 020907
5195431 1007999388 SS MEDROXYPROGESTERONE 1 10 MG, QD UNKNOWN
5195431 1007999389 C EFFEXOR 1 150 MG, UNK
5195431 1007999390 C EFFEXOR 1
5195431 1007999391 C LEVOTHYROXINE /00068002/ 2 88 UG, UNK

Indications of drugs used

Event ID DRUG SEQ INDI PT
5195431 1007999387 MENOPAUSAL SYMPTOMS
5195431 1007999388 MENOPAUSAL SYMPTOMS
5195431 1007999389 DEPRESSION
5195431 1007999390 MENOPAUSAL SYMPTOMS
5195431 1007999391 THYROID DISORDER

Outcome of event

Event ID OUTC COD
5195431 OT

Reactions reported

Event ID PT
5195431 ARTHRITIS
5195431 BREAST CANCER
5195431 BREAST CANCER IN SITU
5195431 DEPRESSION
5195431 OESTROGEN RECEPTOR ASSAY POSITIVE
5195431 PROGESTERONE RECEPTOR ASSAY POSITIVE
5195431 THYROID DISORDER

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
5195431 1007999387 20010101 20030101
5195431 1007999388 20010101
5195431 1007999389 20030801
5195431 1007999391 20030101