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
107873462 10787346 2 F 20160913 20150212 20160914 EXP CA-ROCHE-1536106 ROCHE 62.00 YR F Y 0.00000 20160914 OT CA CA

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
107873462 10787346 1 PS CLONAZEPAM. CLONAZEPAM 1 Unknown U 17533 TABLET
107873462 10787346 2 SS GABAPENTIN. GABAPENTIN 1 Unknown U 0
107873462 10787346 3 SS SANDOSTATIN OCTREOTIDE ACETATE 1 Intramuscular U 0 40 MG
107873462 10787346 4 SS SANDOSTATIN OCTREOTIDE ACETATE 1 Intramuscular U 0 40 MG
107873462 10787346 5 SS SANDOSTATIN OCTREOTIDE ACETATE 1 Intramuscular U 0 40 MG
107873462 10787346 6 C CABERGOLINE. CABERGOLINE 1 Unknown 0 .5 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
107873462 10787346 1 Product used for unknown indication
107873462 10787346 2 Product used for unknown indication
107873462 10787346 3 Acromegaly

Outcome of event

Event ID CASEID OUTC COD
107873462 10787346 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
107873462 10787346 Abdominal discomfort
107873462 10787346 Abdominal pain upper
107873462 10787346 Blood growth hormone increased
107873462 10787346 Blood pressure systolic increased
107873462 10787346 Depression
107873462 10787346 Headache
107873462 10787346 Inappropriate schedule of drug administration
107873462 10787346 Nausea
107873462 10787346 Pain
107873462 10787346 Restless legs syndrome

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

no results found

Therapies reported

no results found