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
127184791 12718479 1 I 201607 20160831 20160906 20160906 EXP US-PFIZER INC-2016413566 PFIZER 44.00 YR F Y 46.72000 KG 20160906 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
127184791 12718479 1 PS REVATIO SILDENAFIL CITRATE 1 20 MG, 3X/DAY (20MG 1 TABLET THREE TIMES A DAY) 21845 20 MG FILM-COATED TABLET TID
127184791 12718479 2 C QVAR BECLOMETHASONE DIPROPIONATE 1 160 UG, 2X/DAY (80 MCG 2 PUFFS 2 TIMES A DAY) 0 160 UG BID
127184791 12718479 3 C QVAR BECLOMETHASONE DIPROPIONATE 1 0
127184791 12718479 4 C BUMEX BUMETANIDE 1 Oral UNK UNK, DAILY (1-2MG BY MOUTH DAILY) 0
127184791 12718479 5 C TUMS CALCIUM CARBONATE 1 200MG 2 TABLETS DAILY AS NEEDED 0 TABLET
127184791 12718479 6 C OSCAL D CALCIUM CARBONATECHOLECALCIFEROL 1 500 MG, 2X/DAY (500MG 1 TABLET TWICE A DAY) 0 500 MG TABLET BID
127184791 12718479 7 C FLOLAN EPOPROSTENOL SODIUM 1 Intravenous (not otherwise specified) 70 NANOGRAMS/KG/MIN CONTINUOUS INTRAVENOUS 0
127184791 12718479 8 C NEURONTIN GABAPENTIN 1 300 MG, 3X/DAY 0 300 MG TID
127184791 12718479 9 C DILAUDID HYDROMORPHONE HYDROCHLORIDE 1 Oral 2 MG, UNK (2MG BY MOUTH EVERY 4 HOURS AS NEEDED) 0 2 MG
127184791 12718479 10 C ALDACTONE SPIRONOLACTONE 1 UNK UNK, 1X/DAY (25MG HALF A TABLET ONCE A DAY) 0 TABLET QD
127184791 12718479 11 C WARFARIN WARFARIN 1 2.5MG 0.5 TO 2 TABLETS AS DIRECTED 0 TABLET
127184791 12718479 12 C OXYGEN. OXYGEN 1 10 LITERS NASAL CANNULA CONTINUOUS AT HOME 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127184791 12718479 1 Pulmonary hypertension
127184791 12718479 2 Dyspnoea
127184791 12718479 3 Chronic respiratory failure
127184791 12718479 4 Oedema
127184791 12718479 5 Dyspepsia
127184791 12718479 6 Mineral supplementation
127184791 12718479 7 Pulmonary hypertension
127184791 12718479 8 Pain
127184791 12718479 9 Pain
127184791 12718479 10 Oedema
127184791 12718479 11 Coagulopathy

Outcome of event

Event ID CASEID OUTC COD
127184791 12718479 HO
127184791 12718479 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
127184791 12718479 Cardiac failure
127184791 12718479 Cardiac failure congestive
127184791 12718479 Chronic respiratory failure
127184791 12718479 Condition aggravated
127184791 12718479 Dyspnoea
127184791 12718479 Hypoxia
127184791 12718479 Pneumonia
127184791 12718479 Pulmonary hypertension
127184791 12718479 Pyrexia
127184791 12718479 Respiratory tract infection

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
127184791 12718479 1 2008 20160827 0