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
126014953 12601495 3 F 20160315 20160829 20160728 20160903 EXP US-AMGEN-USASL2016095293 AMGEN 15.00 YR T M Y 69.00000 KG 20160903 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
126014953 12601495 1 PS SENSIPAR CINACALCET HYDROCHLORIDE 1 Oral 30 MG, BID 21688 30 MG TABLET BID
126014953 12601495 2 SS SENSIPAR CINACALCET HYDROCHLORIDE 1 Unknown 30 MG, TID 21688 30 MG TABLET TID
126014953 12601495 3 C METHYLPHENIDATE. METHYLPHENIDATE 1 UNK 0
126014953 12601495 4 C FAMOTIDINE. FAMOTIDINE 1 10 MG, AS NECESSARY 0 10 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126014953 12601495 1 Hypercalcaemia
126014953 12601495 3 Attention deficit/hyperactivity disorder
126014953 12601495 4 Abdominal discomfort

Outcome of event

Event ID CASEID OUTC COD
126014953 12601495 OT
126014953 12601495 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126014953 12601495 Hospitalisation
126014953 12601495 Hypoaesthesia
126014953 12601495 Off label use

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
126014953 12601495 1 20121220 0
126014953 12601495 3 2012 0
126014953 12601495 4 201208 201308 0