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
104768582 10476858 2 F 201308 20130423 20140926 20160815 EXP US-ROCHE-1425304 ROCHE 17.24 YR M Y 28.00000 KG 20160815 MD 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
104768582 10476858 1 PS NUTROPIN AQ SOMATROPIN 1 Subcutaneous 20522 .8 MG SOLUTION FOR INJECTION QD
104768582 10476858 2 SS NUTROPIN AQ SOMATROPIN 1 Subcutaneous 20522 1 MG SOLUTION FOR INJECTION
104768582 10476858 3 SS CALCITRIOL. CALCITRIOL 1 Unknown U 0 BID
104768582 10476858 4 C LEVOXYL LEVOTHYROXINE SODIUM 1 Unknown 25 MCG 0 25 UG
104768582 10476858 5 C DDAVP DESMOPRESSIN ACETATE 1 Unknown 0 .1 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
104768582 10476858 1 Hypopituitarism
104768582 10476858 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
104768582 10476858 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
104768582 10476858 Asthenia
104768582 10476858 Balance disorder
104768582 10476858 Gait disturbance
104768582 10476858 Hypersensitivity
104768582 10476858 Myalgia
104768582 10476858 Pain in extremity
104768582 10476858 Pollakiuria
104768582 10476858 Polydipsia
104768582 10476858 Polyuria
104768582 10476858 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