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
126405411 12640541 1 I 20160724 20160803 20160810 20160810 PER US-ELI_LILLY_AND_COMPANY-US201608002885 ELI LILLY AND CO 66.00 YR M Y 0.00000 20160810 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
126405411 12640541 1 PS ADCIRCA TADALAFIL 1 Unknown UNK, UNKNOWN U U 21368 TABLET
126405411 12640541 2 SS AMBRISENTAN AMBRISENTAN 1 Unknown 10 MG, QD 0 10 MG TABLET QD
126405411 12640541 3 C PANTOPRAZOLE PANTOPRAZOLE SODIUM 1 0
126405411 12640541 4 C PRAVASTATIN. PRAVASTATIN 1 0
126405411 12640541 5 C METOPROLOL TARTRATE. METOPROLOL TARTRATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126405411 12640541 2 Pulmonary hypertension

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126405411 12640541 Headache
126405411 12640541 Joint swelling
126405411 12640541 Lacrimation increased
126405411 12640541 Nasal congestion

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
126405411 12640541 2 20160724 0