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
121710354 12171035 4 F 20160629 20160311 20160719 PER US-ELI_LILLY_AND_COMPANY-US201602004478 ELI LILLY AND CO 86.00 YR F Y 59.00000 KG 20160719 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
121710354 12171035 1 PS ADCIRCA TADALAFIL 1 Unknown UNK, UNKNOWN U U 21368 TABLET
121710354 12171035 2 SS COUMADIN WARFARIN SODIUM 1 Unknown UNK, UNKNOWN U U 0
121710354 12171035 3 SS AMBRISENTAN AMBRISENTAN 1 Unknown 5 MG, QD U U SBFP 0 5 MG TABLET QD
121710354 12171035 4 C CEFUROXIME. CEFUROXIME 1 Unknown UNK, UNKNOWN U 0
121710354 12171035 5 C LASIX FUROSEMIDE 1 Unknown UNK, UNKNOWN U 0
121710354 12171035 6 C METOLAZONE. METOLAZONE 1 Unknown UNK, UNKNOWN U 0
121710354 12171035 7 C KCL POTASSIUM CHLORIDE 1 Unknown UNK, UNKNOWN U 0
121710354 12171035 8 C SPIRONOLACTONE. SPIRONOLACTONE 1 Unknown UNK, UNKNOWN U 0
121710354 12171035 9 C ACETAMINOPHEN. ACETAMINOPHEN 1 Unknown UNK, UNKNOWN U 0
121710354 12171035 10 C ASCORBIC ACID. ASCORBIC ACID 1 Unknown UNK, UNKNOWN U 0
121710354 12171035 11 C ATORVASTATIN ATORVASTATIN 1 Unknown UNK, UNKNOWN U 0
121710354 12171035 12 C AZELASTINE AZELASTINE 1 Unknown UNK, UNKNOWN U 0
121710354 12171035 13 C CALCIUM CARBONATE AND VITAMIN D 2 Unknown UNK, UNKNOWN U 0
121710354 12171035 14 C CETIRIZINE CETIRIZINE HYDROCHLORIDE 1 Unknown UNK, UNKNOWN U 0
121710354 12171035 15 C COMBIVENT ALBUTEROL SULFATEIPRATROPIUM BROMIDE 1 Unknown UNK, UNKNOWN U 0
121710354 12171035 16 C GLUCOSAMINE + CHONDROITIN /01430901/ 2 0
121710354 12171035 17 C IPRATROPIUM IPRATROPIUM 1 Unknown UNK, UNKNOWN U 0
121710354 12171035 18 C BLISTEX /00530701/ 2 Unknown UNK, UNKNOWN U 0
121710354 12171035 19 C LORAZEPAM. LORAZEPAM 1 Unknown UNK, UNKNOWN U 0
121710354 12171035 20 C METOPROLOL. METOPROLOL 1 Unknown UNK, UNKNOWN U 0
121710354 12171035 21 C EMETROL /00327401/ 2 Unknown UNK, UNKNOWN U 0
121710354 12171035 22 C IMODIUM LOPERAMIDE HYDROCHLORIDE 1 Unknown UNK, UNKNOWN U 0
121710354 12171035 23 C MUPIROCIN. MUPIROCIN 1 Unknown UNK, UNKNOWN U 0
121710354 12171035 24 C LOVAZA OMEGA-3-ACID ETHYL ESTERS 1 Unknown UNK, UNKNOWN U 0
121710354 12171035 25 C OMEPRAZOLE. OMEPRAZOLE 1 Unknown UNK, UNKNOWN U 0
121710354 12171035 26 C FEBUXOSTAT. FEBUXOSTAT 1 Unknown UNK, UNKNOWN U 0
121710354 12171035 27 C ONDANSETRON ONDANSETRON 1 Unknown UNK, UNKNOWN U 0
121710354 12171035 28 C COLCHICINE. COLCHICINE 1 Unknown UNK, UNKNOWN U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121710354 12171035 1 Product used for unknown indication
121710354 12171035 2 Product used for unknown indication
121710354 12171035 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
121710354 12171035 Fluid retention
121710354 12171035 Joint swelling
121710354 12171035 Liver function test increased
121710354 12171035 Malaise
121710354 12171035 Nasal dryness
121710354 12171035 Productive cough
121710354 12171035 Sinusitis
121710354 12171035 Swelling face
121710354 12171035 Weight increased

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
121710354 12171035 3 20131206 0