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
126128651 12612865 1 I 20160727 20160727 20160802 20160802 PER US-ELI_LILLY_AND_COMPANY-US201607013099 ELI LILLY AND CO 0.00 F Y 0.00000 20160802 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
126128651 12612865 1 PS FORTEO TERIPARATIDE 1 Unknown UNK, UNKNOWN 21318 INJECTION
126128651 12612865 2 C DEPAKOTE DIVALPROEX SODIUM 1 U 0
126128651 12612865 3 C LAMICTAL LAMOTRIGINE 1 U 0
126128651 12612865 4 C GABAPENTIN. GABAPENTIN 1 U 0
126128651 12612865 5 C VITAMIN D /07503901/ 2 U 0
126128651 12612865 6 C GLUCOSAMINE CHONDROITIN /01430901/ 2 U 0
126128651 12612865 7 C SYNTHROID LEVOTHYROXINE SODIUM 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126128651 12612865 1 Osteoporosis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126128651 12612865 Abdominal pain upper
126128651 12612865 Arthralgia
126128651 12612865 Asthenia
126128651 12612865 Blood calcium increased
126128651 12612865 Constipation
126128651 12612865 Hyperhidrosis
126128651 12612865 Muscular weakness

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

no results found

Therapies reported

no results found