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
127763421 12776342 1 I 2015 20160919 20160923 20160923 PER US-PFIZER INC-2016440607 PFIZER 71.00 YR F Y 48.60000 KG 20160923 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
127763421 12776342 1 PS GABAPENTIN. GABAPENTIN 1 100 MG, 1X/DAY N 20235 100 MG CAPSULE, HARD QD
127763421 12776342 2 SS GABAPENTIN. GABAPENTIN 1 300 MG, 2X/DAY N 20235 300 MG CAPSULE, HARD BID
127763421 12776342 3 SS GABAPENTIN. GABAPENTIN 1 Oral 100 MG, 3X/DAY N 20235 100 MG CAPSULE, HARD TID
127763421 12776342 4 SS GABAPENTIN. GABAPENTIN 1 300 MG, 2X/DAY N 20235 300 MG CAPSULE, HARD BID
127763421 12776342 5 SS GABAPENTIN. GABAPENTIN 1 100 MG, 2X/DAY N 20235 100 MG CAPSULE, HARD BID
127763421 12776342 6 SS GABAPENTIN. GABAPENTIN 1 100 MG, UNK (ONCE) N 20235 100 MG CAPSULE, HARD
127763421 12776342 7 SS GABAPENTIN. GABAPENTIN 1 200 MG, UNK (TOOK TWO 100MG ONCE THAT DAY) N 20235 200 MG CAPSULE, HARD
127763421 12776342 8 SS GABAPENTIN. GABAPENTIN 1 600 MG, UNK N 20235 600 MG CAPSULE, HARD
127763421 12776342 9 SS LYRICA PREGABALIN 1 75 MG, 2X/DAY U 21446 75 MG CAPSULE, HARD BID
127763421 12776342 10 SS LYRICA PREGABALIN 1 50 MG, UNK U 21446 50 MG CAPSULE, HARD
127763421 12776342 11 SS LYRICA PREGABALIN 1 50 MG, 2X/DAY U 21446 50 MG CAPSULE, HARD BID
127763421 12776342 12 SS LYRICA PREGABALIN 1 50 MG, (ONE CAPSULE) U 21446 50 MG CAPSULE, HARD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127763421 12776342 1 Neuropathy peripheral
127763421 12776342 2 Neuralgia
127763421 12776342 3 Headache
127763421 12776342 9 Neuralgia

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127763421 12776342 Condition aggravated
127763421 12776342 Drug ineffective for unapproved indication
127763421 12776342 Drug intolerance
127763421 12776342 Feeling abnormal
127763421 12776342 Head discomfort
127763421 12776342 Headache
127763421 12776342 Intentional product misuse
127763421 12776342 Neuralgia
127763421 12776342 Tinnitus

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
127763421 12776342 2 2015 0
127763421 12776342 3 201607 20160917 0
127763421 12776342 4 201608 0
127763421 12776342 5 20160914 0
127763421 12776342 6 20160915 0
127763421 12776342 7 20160916 0
127763421 12776342 9 2015 0
127763421 12776342 12 20160918 0