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
107082648 10708264 8 F 20140925 20160824 20150113 20160831 EXP US-PFIZER INC-2015010837 PFIZER 81.00 YR F Y 61.23000 KG 20160831 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
107082648 10708264 1 PS REVATIO SILDENAFIL CITRATE 1 Oral 20 MG, 3X/DAY A410702 21845 20 MG FILM-COATED TABLET TID
107082648 10708264 2 SS REVATIO SILDENAFIL CITRATE 1 Oral 20 MG, 3X/DAY A440301 21845 20 MG FILM-COATED TABLET TID
107082648 10708264 3 SS REVATIO SILDENAFIL CITRATE 1 Oral 20 MG, 3X/DAY A563501 21845 20 MG FILM-COATED TABLET TID
107082648 10708264 4 SS FLU INFLUENZA VIRUS VACCINE 1 0
107082648 10708264 5 C SYNTHROID LEVOTHYROXINE SODIUM 1 Oral 100 MG, 1X/DAY 0 100 MG TABLET QD
107082648 10708264 6 C FOLIC ACID. FOLIC ACID 1 Oral 1 MG, 1X/DAY 0 1 MG TABLET QD
107082648 10708264 7 C IRBESARTAN. IRBESARTAN 1 Oral 300 MG, 1X/DAY 0 300 MG TABLET QD
107082648 10708264 8 C COLACE DOCUSATE SODIUM 1 UNK 0
107082648 10708264 9 C SENNA SENNA LEAFSENNOSIDESSENNOSIDES A AND B 1 UNK 0
107082648 10708264 10 C VITAMIN D3 CHOLECALCIFEROL 1 Oral 2000 IU, DAILY 0 2000 IU TABLET
107082648 10708264 11 C VITAMIN B6 PYRIDOXINE HYDROCHLORIDE 1 Oral 50 MG, DAILY 0 50 MG TABLET
107082648 10708264 12 C VITAMIN B12 CYANOCOBALAMIN 1 1000 UG/ML, MONTHLY (ONE INJECTION IN THE RIGHT ARM ONCE A MONTH) 0 INJECTION /month
107082648 10708264 13 C NAPROXEN. NAPROXEN 1 UNK 0
107082648 10708264 14 C ZYRTEC CETIRIZINE HYDROCHLORIDE 1 UNK 0
107082648 10708264 15 C NAPRO 2 0
107082648 10708264 16 C TYLENOL ACETAMINOPHEN 1 Oral 325 MG, AS NEEDED (WHEN NEEDED) 0 325 MG TABLET
107082648 10708264 17 C TYLENOL ACETAMINOPHEN 1 0 TABLET
107082648 10708264 18 C TYLENOL ACETAMINOPHEN 1 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
107082648 10708264 1 Pulmonary arterial hypertension
107082648 10708264 2 Pulmonary hypertension
107082648 10708264 5 Hypothyroidism
107082648 10708264 6 Blood disorder
107082648 10708264 7 Hypertension
107082648 10708264 10 Supplementation therapy
107082648 10708264 11 Supplementation therapy
107082648 10708264 12 Blood homocysteine
107082648 10708264 16 Injury
107082648 10708264 17 Fatigue
107082648 10708264 18 Pain

Outcome of event

Event ID CASEID OUTC COD
107082648 10708264 HO
107082648 10708264 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
107082648 10708264 Blood count abnormal
107082648 10708264 Cough
107082648 10708264 Fall
107082648 10708264 Hip fracture
107082648 10708264 Malaise
107082648 10708264 Pelvic fracture
107082648 10708264 Pneumonia

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
107082648 10708264 1 20050109 0
107082648 10708264 2 2004 0
107082648 10708264 3 2005 0
107082648 10708264 5 19970722 0
107082648 10708264 10 2004 0
107082648 10708264 11 2004 0
107082648 10708264 12 2005 0
107082648 10708264 16 2004 0