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
112341014 11234101 4 F 201412 20160919 20150702 20160922 EXP US-PFIZER INC-2015213569 PFIZER 57.00 YR F Y 58.96000 KG 20160922 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
112341014 11234101 1 PS LYRICA PREGABALIN 1 Oral 1 DF, 2X/DAY D 136914 21446 1 DF CAPSULE, HARD BID
112341014 11234101 2 SS LYRICA PREGABALIN 1 Oral 150 MG, 2X/DAY D 21446 150 MG CAPSULE, HARD BID
112341014 11234101 3 SS LYRICA PREGABALIN 1 Oral 3 DF, UNK D 21446 3 DF CAPSULE, HARD
112341014 11234101 4 SS LYRICA PREGABALIN 1 Oral 150 MG, 3X/DAY (10:00 AM, 04:00 PM,10:00 PM.) D L75535 21446 150 MG CAPSULE, HARD TID
112341014 11234101 5 SS LYRICA PREGABALIN 1 UNK D 21446 CAPSULE, HARD
112341014 11234101 6 SS LYRICA PREGABALIN 1 Oral 200 MG, 2X/DAY D N42775 21446 200 MG CAPSULE, HARD BID
112341014 11234101 7 C XANAX ALPRAZOLAM 1 UNK, DAILY 0
112341014 11234101 8 C ZOLOFT SERTRALINE HYDROCHLORIDE 1 50 MG, 1X/DAY 0 50 MG TABLET QD
112341014 11234101 9 C ZOLOFT SERTRALINE HYDROCHLORIDE 1 Oral 100 MG, 1X/DAY 0 100 MG TABLET QD
112341014 11234101 10 C METFORMIN HYDROCHLORIDE. METFORMIN HYDROCHLORIDE 1 500 MG, DAILY 0 500 MG
112341014 11234101 11 C CYMBALTA DULOXETINE HYDROCHLORIDE 1 Oral 60 MG, 1X/DAY 0 60 MG TABLET QD
112341014 11234101 12 C BABY ASPIRIN ASPIRIN 1 Oral 2 DF, DAILY 0 2 DF CHEWABLE TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
112341014 11234101 1 Neuropathy peripheral
112341014 11234101 2 Pain in extremity
112341014 11234101 8 Anxiety
112341014 11234101 11 Anxiety
112341014 11234101 12 Pain

Outcome of event

Event ID CASEID OUTC COD
112341014 11234101 OT
112341014 11234101 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
112341014 11234101 Anxiety
112341014 11234101 Asthenia
112341014 11234101 Confusional state
112341014 11234101 Crying
112341014 11234101 Depression
112341014 11234101 Drug dose omission
112341014 11234101 Drug ineffective
112341014 11234101 Eating disorder
112341014 11234101 Fall
112341014 11234101 Headache
112341014 11234101 Limb discomfort
112341014 11234101 Memory impairment
112341014 11234101 Muscle spasms
112341014 11234101 Pain
112341014 11234101 Pain in extremity
112341014 11234101 Sleep disorder
112341014 11234101 Suicidal ideation
112341014 11234101 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
112341014 11234101 1 2015 0
112341014 11234101 4 201412 0
112341014 11234101 5 201608 0
112341014 11234101 6 2014 0
112341014 11234101 8 20150319 0
112341014 11234101 9 20160830 0
112341014 11234101 11 20160830 0
112341014 11234101 12 2015 0