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
126729171 12672917 1 I 201603 20160810 20160822 20160822 EXP FR-NOVOPROD-505765 NOVO NORDISK 77.00 YR E F Y 0.00000 20160822 OT FR FR

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
126729171 12672917 1 PS NovoNorm REPAGLINIDE 1 Unknown 6 DF, QD Y N UNKNOWN 20741 6 DF TABLET QD
126729171 12672917 2 SS NovoNorm REPAGLINIDE 1 Unknown 1MG 2 TIMES A DAY AT NOON AND IN EVENING Y N UNKNOWN 20741 TABLET
126729171 12672917 3 SS STAGID METFORMIN PAMOATE 1 Oral 3 DF, QD Y U UNKNOWN 0 3 DF QD
126729171 12672917 4 SS ONGLYZA SAXAGLIPTIN HYDROCHLORIDE 1 Oral 1 DF, QD Y U UNKNOWN 0 1 DF QD
126729171 12672917 5 SS ALDACTONE SPIRONOLACTONE 1 Oral 1 DF, QD Y U UNKNOWN 0 1 DF QD
126729171 12672917 6 C SIMVASTATINE SIMVASTATIN 1 Unknown UNK 0
126729171 12672917 7 C AVLOCARDYL /00030001/ PROPRANOLOL HYDROCHLORIDE 1 Unknown UNK 0
126729171 12672917 8 C TRIATEC /00116401/ ACETAMINOPHENCODEINE PHOSPHATE 1 Unknown UNK 0
126729171 12672917 9 C KARDEGIC ASPIRIN LYSINE 1 Unknown UNK 0
126729171 12672917 10 C LANTUS INSULIN GLARGINE 1 Unknown UNK 0
126729171 12672917 11 C PANTOPRAZOLE PANTOPRAZOLE SODIUM 1 Unknown UNK 0
126729171 12672917 12 C LERCAN LERCANIDIPINE 1 Unknown UNK 0
126729171 12672917 13 C DOLIPRANE ACETAMINOPHEN 1 Unknown UNK 0
126729171 12672917 14 C DUROGESIC FENTANYL 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126729171 12672917 1 Type 2 diabetes mellitus
126729171 12672917 3 Type 2 diabetes mellitus
126729171 12672917 4 Type 2 diabetes mellitus
126729171 12672917 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126729171 12672917 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126729171 12672917 Abdominal pain
126729171 12672917 Diarrhoea

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
126729171 12672917 1 20160309 0
126729171 12672917 2 20160311 20160313 0
126729171 12672917 3 20160309 0
126729171 12672917 4 20160309 0
126729171 12672917 5 20160309 0