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
127063941 12706394 1 I 200807 20160826 20160901 20160901 EXP US-JNJFOC-20160823238 JOHNSON AND JOHNSON 77.47 YR E F Y 0.00000 20160901 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
127063941 12706394 1 PS IMODIUM LOPERAMIDE HYDROCHLORIDE 1 Unknown U U 19487 UNSPECIFIED
127063941 12706394 2 SS IMODIUM LOPERAMIDE HYDROCHLORIDE 1 Unknown U U 19487 2 MG UNSPECIFIED QD
127063941 12706394 3 SS REVATIO SILDENAFIL CITRATE 1 Unknown Y 0 UNSPECIFIED
127063941 12706394 4 SS VIAGRA SILDENAFIL CITRATE 1 Unknown U 0 UNSPECIFIED
127063941 12706394 5 SS LEVOTHYROXINE SODIUM. LEVOTHYROXINE SODIUM 1 Unknown 0 75 UG UNSPECIFIED QD
127063941 12706394 6 SS FUROSEMIDE. FUROSEMIDE 1 Unknown 0 20 MG UNSPECIFIED QD
127063941 12706394 7 SS DIGOXIN. DIGOXIN 1 Unknown 0 125 UG UNSPECIFIED QD
127063941 12706394 8 SS FLOLAN EPOPROSTENOL SODIUM 1 Unknown 0 50 ML UNSPECIFIED
127063941 12706394 9 SS LETAIRIS AMBRISENTAN 1 Unknown 0 5 UG UNSPECIFIED QD
127063941 12706394 10 SS COUMADIN WARFARIN SODIUM 1 Unknown Y 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127063941 12706394 2 Pulmonary arterial hypertension
127063941 12706394 3 Pulmonary arterial hypertension
127063941 12706394 4 Product used for unknown indication
127063941 12706394 5 Pulmonary arterial hypertension
127063941 12706394 6 Pulmonary arterial hypertension
127063941 12706394 7 Pulmonary arterial hypertension
127063941 12706394 8 Pulmonary arterial hypertension
127063941 12706394 9 Pulmonary arterial hypertension
127063941 12706394 10 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127063941 12706394 HO
127063941 12706394 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127063941 12706394 Anaemia
127063941 12706394 Diarrhoea
127063941 12706394 Fall
127063941 12706394 Hip fracture
127063941 12706394 Joint swelling
127063941 12706394 Product use issue

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
127063941 12706394 10 2015 0