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
1211870415 12118704 15 F 20150615 20160822 20160226 20160824 EXP US-ELI_LILLY_AND_COMPANY-US201602000956 ELI LILLY AND CO 54.69 YR F Y 51.00000 KG 20160824 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
1211870415 12118704 1 PS ADCIRCA TADALAFIL 1 Unknown 40 MG, UNKNOWN U U 21368 40 MG TABLET
1211870415 12118704 2 SS REVATIO SILDENAFIL CITRATE 1 Oral 80 MG, TID 0 80 MG TABLET
1211870415 12118704 3 SS REVATIO SILDENAFIL CITRATE 1 Oral UNK 0 TABLET
1211870415 12118704 4 SS LETAIRIS AMBRISENTAN 1 Oral 5 MG, QD SBFT 0 5 MG TABLET QD
1211870415 12118704 5 SS LETAIRIS AMBRISENTAN 1 Oral 10 MG, QD 1500226A 0 10 MG TABLET QD
1211870415 12118704 6 SS LETAIRIS AMBRISENTAN 1 Oral 20 MG, QD SBFX 0 20 MG TABLET QD
1211870415 12118704 7 SS LETAIRIS AMBRISENTAN 1 Unknown 10 MG, QD SBFT 0 10 MG TABLET QD
1211870415 12118704 8 SS LETAIRIS AMBRISENTAN 1 Unknown 5 MG, QD NZYD 0 5 MG TABLET QD
1211870415 12118704 9 SS REMODULIN TREPROSTINIL 1 Intravenous (not otherwise specified) 0.097 ?G/KG, UNKNOWN 2100578 0 .097 UG/KG
1211870415 12118704 10 SS REMODULIN TREPROSTINIL 1 Intravenous (not otherwise specified) 0.099 ?G/KG, UNKNOWN 926117 0 .099 UG/KG
1211870415 12118704 11 SS REMODULIN TREPROSTINIL 1 Intravenous (not otherwise specified) UNK UNK, UNKNOWN 926117 0
1211870415 12118704 12 SS REMODULIN TREPROSTINIL 1 Intravenous (not otherwise specified) 0.100 ?G/KG, UNKNOWN 2100703 0 .1 UG/KG
1211870415 12118704 13 SS REMODULIN TREPROSTINIL 1 Intravenous (not otherwise specified) 99 NG/KG/MIN, UNKNOWN 926618 0
1211870415 12118704 14 SS REMODULIN TREPROSTINIL 1 Intravenous (not otherwise specified) 94 NG/KG/MIN, OTHER 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
1211870415 12118704 1 Pulmonary arterial hypertension
1211870415 12118704 2 Osteopenia
1211870415 12118704 3 Pulmonary arterial hypertension
1211870415 12118704 4 Pulmonary arterial hypertension
1211870415 12118704 9 Pulmonary arterial hypertension

Outcome of event

Event ID CASEID OUTC COD
1211870415 12118704 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
1211870415 12118704 Asthma
1211870415 12118704 Bacteraemia
1211870415 12118704 Bacterial infection
1211870415 12118704 Blood immunoglobulin E increased
1211870415 12118704 Bronchopulmonary aspergillosis
1211870415 12118704 Chronic obstructive pulmonary disease
1211870415 12118704 Cough
1211870415 12118704 Dyspnoea
1211870415 12118704 Eye discharge
1211870415 12118704 Fungal infection
1211870415 12118704 Headache
1211870415 12118704 Insomnia
1211870415 12118704 Malaise
1211870415 12118704 Muscle spasms
1211870415 12118704 Nasopharyngitis
1211870415 12118704 Nausea
1211870415 12118704 Ocular hyperaemia
1211870415 12118704 Osteopenia
1211870415 12118704 Osteoporosis
1211870415 12118704 Upper respiratory tract infection
1211870415 12118704 Urinary tract infection
1211870415 12118704 Weight decreased

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
1211870415 12118704 4 20150410 0
1211870415 12118704 5 20150410 0
1211870415 12118704 6 20151028 0
1211870415 12118704 9 20150409 0
1211870415 12118704 13 20150409 0