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
126895141 12689514 1 I 201308 20130423 20160826 20160826 EXP US-VALIDUS PHARMACEUTICALS LLC-US-2013VAL000655 VALIDUS 0.00 Y 0.00000 20160826 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
126895141 12689514 1 PS CALCITRIOL. CALCITRIOL 1 2 IN 1 D U 18044
126895141 12689514 2 SS NUTROPIN AQ SOMATROPIN 1 Subcutaneous 0.8 MG,1 IN 1 D 0 .8 MG SOLUTION FOR INJECTION
126895141 12689514 3 SS NUTROPIN AQ SOMATROPIN 1 Subcutaneous 1 MG,7 IN 1 WK 0 SOLUTION FOR INJECTION
126895141 12689514 4 C LEVOXYL LEVOTHYROXINE SODIUM 1 25 ?G, UNK U 0 25 UG
126895141 12689514 5 C DDAVP DESMOPRESSIN ACETATE 1 0.1 MG, UNK U 0 .1 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126895141 12689514 1 Product used for unknown indication
126895141 12689514 2 Hypopituitarism
126895141 12689514 4 Product used for unknown indication
126895141 12689514 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126895141 12689514 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126895141 12689514 Asthenia
126895141 12689514 Balance disorder
126895141 12689514 Gait disturbance
126895141 12689514 Hypersensitivity
126895141 12689514 Myalgia
126895141 12689514 Pain in extremity
126895141 12689514 Pollakiuria
126895141 12689514 Polydipsia
126895141 12689514 Polyuria
126895141 12689514 Sleep apnoea syndrome

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

no results found

Therapies reported

no results found