The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
5577899 6517134 I 5577899-9 20071201 20071218 20071231 EXP ES-ELI_LILLY_AND_COMPANY-ES200712003826 ELI LILLY AND COMPANY 69 YR F Y 20071221 CN SPAIN

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
5577899 1009350011 PS FORTEO 1 SUBCUTANEOUS 20 UG, UNKNOWN 021318
5577899 1009350012 C ADIRO 2 UNKNOWN UNK, UNKNOWN
5577899 1009350013 C CITALOPRAM HYDROBROMIDE 1 UNKNOWN UNK, UNKNOWN
5577899 1009350014 C ANTIBIOTICS 2 UNKNOWN UNK, UNKNOWN

Indications of drugs used

Event ID DRUG SEQ INDI PT
5577899 1009350011 OSTEOPOROSIS
5577899 1009350012 PLATELET COUNT INCREASED
5577899 1009350014 EAR INFECTION

Outcome of event

Event ID OUTC COD
5577899 HO

Reactions reported

Event ID PT
5577899 ASTHENIA
5577899 BEDRIDDEN
5577899 DIARRHOEA
5577899 FALL
5577899 PLEURAL EFFUSION

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

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
5577899 1009350011 20070301