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
106574983 10657498 3 F 20160729 20141217 20160802 PER US-PFIZER INC-2014341454 PFIZER 83.00 YR F Y 0.00000 20160802 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
106574983 10657498 1 PS LYRICA PREGABALIN 1 50 MG, 2X/DAY (ONE IN AM AND ONE IN THE PM) 21446 50 MG CAPSULE, HARD BID
106574983 10657498 2 SS LYRICA PREGABALIN 1 50 MG, 3X/DAY (ONE IN THE AM AND TWO AT NIGHT) 21446 50 MG CAPSULE, HARD TID
106574983 10657498 3 SS LYRICA PREGABALIN 1 UNK, 3X/DAY (200, 1 AT MORNING AND 2 AT BEDTIME) 21446 CAPSULE, HARD TID
106574983 10657498 4 C CYMBALTA DULOXETINE HYDROCHLORIDE 1 UNK 0
106574983 10657498 5 C CYMBALTA DULOXETINE HYDROCHLORIDE 1 0
106574983 10657498 6 C XANAX ALPRAZOLAM 1 0.5 MG, UNK 0 .5 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
106574983 10657498 1 Fibromyalgia
106574983 10657498 4 Rheumatoid arthritis
106574983 10657498 5 Osteoporosis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
106574983 10657498 Condition aggravated
106574983 10657498 Drug ineffective
106574983 10657498 Pain
106574983 10657498 Prescribed overdose
106574983 10657498 Somnolence

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found