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
125747072 12574707 2 F 2015 20160802 20160720 20160808 EXP US-PFIZER INC-2016344924 PFIZER 41.00 YR F Y 74.39000 KG 20160808 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
125747072 12574707 1 PS IBUPROFEN. IBUPROFEN 1 Oral 800 MG, 4X/DAY Y 18989 800 MG TABLET QID
125747072 12574707 2 C ZANAFLEX TIZANIDINE HYDROCHLORIDE 1 4 DF, DAILY 0 4 DF TABLET
125747072 12574707 3 C GABAPENTIN. GABAPENTIN 1 Oral 200 MG, 1X/DAY AT NIGHT BEFORE BED 0 200 MG CAPSULE QD
125747072 12574707 4 C PERCOCET ACETAMINOPHENOXYCODONE HYDROCHLORIDE 1 Oral 10 MG, 4X/DAY 0 10 MG TABLET QID
125747072 12574707 5 C KLONOPIN CLONAZEPAM 1 Oral 1 MG, 1X/DAY AT NIGHT 0 1 MG TABLET QD
125747072 12574707 6 C CENTRAMIN 2 Oral 37.5 MG, 1X/DAY 0 37.5 MG TABLET QD
125747072 12574707 7 C VITAMIN D CHOLECALCIFEROL 1 5000 IU, WEEKLY 0 5000 IU /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125747072 12574707 1 Osteoarthritis
125747072 12574707 2 Muscle spasms
125747072 12574707 3 Neuralgia
125747072 12574707 4 Back pain
125747072 12574707 5 Anxiety
125747072 12574707 6 Weight decreased

Outcome of event

Event ID CASEID OUTC COD
125747072 12574707 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125747072 12574707 Gastric haemorrhage
125747072 12574707 Overdose
125747072 12574707 Renal impairment

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

no results found

Therapies reported

no results found