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
126140431 12614043 1 I 20160317 0 20160801 20160801 DIR 50.00 YR F N 126.00000 LBS 20160731 Y 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
126140431 12614043 1 PS LORAZEPAM. LORAZEPAM 1 Oral Y Y 20170630 0 60 DF COATED TABLET BID
126140431 12614043 2 C VIVELLE-DOT ESTRADIOL 1 0
126140431 12614043 3 C PREMARIN ESTROGENS, CONJUGATED 1 0
126140431 12614043 4 C PREDNISONE. PREDNISONE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126140431 12614043 1 Anxiety

Outcome of event

Event ID CASEID OUTC COD
126140431 12614043 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126140431 12614043 Arthralgia
126140431 12614043 Back pain
126140431 12614043 Dyspnoea
126140431 12614043 Malaise
126140431 12614043 Mobility decreased
126140431 12614043 Muscle spasms
126140431 12614043 Paraesthesia
126140431 12614043 Urinary retention
126140431 12614043 Vision blurred
126140431 12614043 Vomiting

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
126140431 12614043 1 20160317 20160321 0