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
1062337611 10623376 11 F 20130706 20160926 20141203 20160930 EXP US-PFIZER INC-2014330899 PFIZER 72.00 YR F Y 73.00000 KG 20160930 OT 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
1062337611 10623376 1 PS LYRICA PREGABALIN 1 4 DF, DAILY D 21446 4 DF CAPSULE, HARD
1062337611 10623376 2 SS LYRICA PREGABALIN 1 3 DF, DAILY D 21446 3 DF CAPSULE, HARD
1062337611 10623376 3 SS LYRICA PREGABALIN 1 75 MG, QD (EVERYDAY) D 21446 75 MG CAPSULE, HARD QD
1062337611 10623376 4 SS LYRICA PREGABALIN 1 75 MG, 4X/DAY D 21446 75 MG CAPSULE, HARD QID
1062337611 10623376 5 SS LYRICA PREGABALIN 1 50 MG, UNK D 21446 50 MG CAPSULE, HARD
1062337611 10623376 6 SS LYRICA PREGABALIN 1 Oral 50 MG, 4X/DAY D M22818 21446 50 MG CAPSULE, HARD QID
1062337611 10623376 7 C OXYCODONE OXYCODONE 1 15 MG, 4X/DAY (CUTS IN HALF) 0 15 MG QID
1062337611 10623376 8 C LEVOTHYROXINE. LEVOTHYROXINE 1 125 MG, 1X/DAY 0 125 MG QD
1062337611 10623376 9 C TYLENOL ACETAMINOPHEN 1 650 MG, 2X/DAY 0 650 MG BID
1062337611 10623376 10 C TYLENOL ACETAMINOPHEN 1 0
1062337611 10623376 11 C IBUPROFEN. IBUPROFEN 1 200 MG, UNK 0 200 MG
1062337611 10623376 12 C FISH OIL FISH OIL 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
1062337611 10623376 1 Neuralgia
1062337611 10623376 2 Pain
1062337611 10623376 7 Spinal operation
1062337611 10623376 8 Thyroid disorder
1062337611 10623376 9 Analgesic therapy
1062337611 10623376 10 Arthritis
1062337611 10623376 11 Analgesic therapy
1062337611 10623376 12 Arthropathy

Outcome of event

Event ID CASEID OUTC COD
1062337611 10623376 OT
1062337611 10623376 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
1062337611 10623376 Amnesia
1062337611 10623376 Back pain
1062337611 10623376 Discomfort
1062337611 10623376 Drug effect incomplete
1062337611 10623376 Drug intolerance
1062337611 10623376 Feeling abnormal
1062337611 10623376 Hallucination
1062337611 10623376 Intentional product use issue
1062337611 10623376 Mental disorder
1062337611 10623376 Nerve injury
1062337611 10623376 Pain in extremity
1062337611 10623376 Peripheral coldness
1062337611 10623376 Somnolence
1062337611 10623376 Vertebral lesion

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
1062337611 10623376 3 2013 0
1062337611 10623376 6 2014 20160915 0
1062337611 10623376 7 2005 0
1062337611 10623376 8 1995 0