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
125397512 12539751 2 F 20160604 20160811 20160708 20160815 EXP US-PFIZER INC-2016306162 PFIZER 67.00 YR F Y 0.00000 20160815 MD 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
125397512 12539751 1 PS SILDENAFIL CITRATE. SILDENAFIL CITRATE 1 UNK UNK, 2X/DAY U 21845 FILM-COATED TABLET BID
125397512 12539751 2 SS LETAIRIS AMBRISENTAN 1 4.5 MG, 1X/DAY U 1412805A 0 4.5 MG TABLET QD
125397512 12539751 3 SS LETAIRIS AMBRISENTAN 1 5 MG, DAILY U 1412805A 0 5 MG TABLET
125397512 12539751 4 SS ADCIRCA TADALAFIL 1 UNK, 2X/DAY U 0
125397512 12539751 5 SS REMODULIN TREPROSTINIL 1 Subcutaneous 0.010 UG/KG, (2.5MG/ML) (10.25 NG/KG/MIN) 0 .01 UG/KG INJECTION
125397512 12539751 6 SS REMODULIN TREPROSTINIL 1 Subcutaneous 10.25 MG/KG, UNK (10.25 NG/KG/MIN) 0 10.25 MG/KG INJECTION
125397512 12539751 7 SS REMODULIN TREPROSTINIL 1 Subcutaneous 0.010 UG/KG, (2.5MG/ML) (10.25 NG/KG/MIN) 0 .011 UG/KG INJECTION
125397512 12539751 8 SS UPTRAVI SELEXIPAG 1 UNK UNK, 2X/DAY U 0 BID
125397512 12539751 9 SS UPTRAVI SELEXIPAG 1 U 0
125397512 12539751 10 C TORSEMIDE. TORSEMIDE 1 UNK 0
125397512 12539751 11 C CYCLOBENZAPRINE CYCLOBENZAPRINE 1 UNK 0
125397512 12539751 12 C NORVASC AMLODIPINE BESYLATE 1 UNK 0
125397512 12539751 13 C PROTONIX PANTOPRAZOLE SODIUM 1 UNK 0
125397512 12539751 14 C GLIPIZIDE. GLIPIZIDE 1 UNK 0
125397512 12539751 15 C METOPROLOL. METOPROLOL 1 UNK 0
125397512 12539751 16 C DIGOXIN. DIGOXIN 1 UNK 0
125397512 12539751 17 C FENOFIBRATE. FENOFIBRATE 1 UNK 0
125397512 12539751 18 C DIAZEPAM. DIAZEPAM 1 UNK 0
125397512 12539751 19 C TRAVATAN Z TRAVOPROST 1 UNK 0
125397512 12539751 20 C PRILOSEC OMEPRAZOLE MAGNESIUM 1 UNK 0
125397512 12539751 21 C DEPO-MEDROL METHYLPREDNISOLONE ACETATE 1 UNK 0
125397512 12539751 22 C KLOR-CON POTASSIUM CHLORIDE 1 UNK 0
125397512 12539751 23 C RESTASIS CYCLOSPORINE 1 UNK 0
125397512 12539751 24 C PERCOCET ACETAMINOPHENOXYCODONE HYDROCHLORIDE 1 UNK 0
125397512 12539751 25 C METOPROLOL SUCCINATE. METOPROLOL SUCCINATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125397512 12539751 1 Pulmonary hypertension
125397512 12539751 2 Pulmonary arterial hypertension
125397512 12539751 4 Pulmonary hypertension
125397512 12539751 5 Pulmonary arterial hypertension
125397512 12539751 8 Pulmonary arterial hypertension
125397512 12539751 9 Pulmonary hypertension

Outcome of event

Event ID CASEID OUTC COD
125397512 12539751 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125397512 12539751 Dizziness
125397512 12539751 Fall
125397512 12539751 Headache
125397512 12539751 Myalgia
125397512 12539751 Nausea

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
125397512 12539751 1 20160613 0
125397512 12539751 2 20160607 0
125397512 12539751 3 20160607 0
125397512 12539751 5 20160505 0
125397512 12539751 6 20160415 20160616 0
125397512 12539751 7 20160613 0
125397512 12539751 8 20160613 0