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
125898601 12589860 1 I 20160513 20160714 20160725 20160725 EXP US-ELI_LILLY_AND_COMPANY-US201607005603 ELI LILLY AND CO 60.00 YR F Y 0.00000 20160725 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
125898601 12589860 1 PS EFFIENT PRASUGREL HYDROCHLORIDE 1 Unknown UNK, UNKNOWN 22307 TABLET
125898601 12589860 2 SS EFFIENT PRASUGREL HYDROCHLORIDE 1 Unknown 10 MG, QD C510204A 22307 10 MG TABLET QD
125898601 12589860 3 SS AGRASTAT TIROFIBAN HYDROCHLORIDE 1 Unknown UNK UNK, UNKNOWN U U 0
125898601 12589860 4 SS ATARAX HYDROXYZINEHYDROXYZINE HYDROCHLORIDE 1 Unknown UNK, UNKNOWN U U 0
125898601 12589860 5 C ASPIRIN 81 ASPIRIN 1 0
125898601 12589860 6 C ALLEGRA FEXOFENADINE HYDROCHLORIDE 1 0
125898601 12589860 7 C ELMIRON PENTOSAN POLYSULFATE SODIUM 1 0
125898601 12589860 8 C ZANTAC RANITIDINE HYDROCHLORIDE 1 0
125898601 12589860 9 C PREMARIN ESTROGENS, CONJUGATED 1 0
125898601 12589860 10 C PROTONIX /00661201/ OMEPRAZOLE 1 0
125898601 12589860 11 C PYRIDIUM PHENAZOPYRIDINE 1 0
125898601 12589860 12 C CARAFATE SUCRALFATE 1 0
125898601 12589860 13 C TYLENOL EXTRA STRENGTH ACETAMINOPHEN 1 0
125898601 12589860 14 C PRAVACHOL PRAVASTATIN SODIUM 1 0
125898601 12589860 15 C VALIUM DIAZEPAM 1 UNK, PRN 0
125898601 12589860 16 C FLUCONAZOLE. FLUCONAZOLE 1 0
125898601 12589860 17 C BUDESONIDE. BUDESONIDE 1 0
125898601 12589860 18 C SUDAFED PSEUDOEPHEDRINE HYDROCHLORIDE 1 0
125898601 12589860 19 C TUMS /00193601/ CALCIUM CARBONATEMAGNESIUM CARBONATEMAGNESIUM TRISILICATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125898601 12589860 1 Stent placement
125898601 12589860 3 Product used for unknown indication
125898601 12589860 4 Pruritus
125898601 12589860 5 Product used for unknown indication
125898601 12589860 6 Product used for unknown indication
125898601 12589860 7 Product used for unknown indication
125898601 12589860 8 Product used for unknown indication
125898601 12589860 9 Product used for unknown indication
125898601 12589860 10 Product used for unknown indication
125898601 12589860 11 Product used for unknown indication
125898601 12589860 12 Product used for unknown indication
125898601 12589860 13 Product used for unknown indication
125898601 12589860 14 Product used for unknown indication
125898601 12589860 15 Product used for unknown indication
125898601 12589860 16 Product used for unknown indication
125898601 12589860 17 Product used for unknown indication
125898601 12589860 18 Product used for unknown indication
125898601 12589860 19 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125898601 12589860 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125898601 12589860 Haemoglobin decreased
125898601 12589860 Hypersomnia
125898601 12589860 Post procedural haemorrhage
125898601 12589860 Pruritus
125898601 12589860 Subcutaneous haematoma

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
125898601 12589860 1 2014 2014 0
125898601 12589860 2 20160513 0
125898601 12589860 3 20160513 0