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
127311431 12731143 1 I 20151117 0 20160909 20160909 DIR US-FDA-350136 FDA-CTU 50.00 YR F N 72.00000 KG 20160909 N 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
127311431 12731143 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 Oral N D 0 BID
127311431 12731143 2 C BIO-IDENTICAL PROGESTERONE 2 0
127311431 12731143 3 C ESTRIOL/ESTRADIOL 2 0
127311431 12731143 5 C IBUPROFEN. IBUPROFEN 1 0
127311431 12731143 7 C MULTIVITAMINS VITAMINS 1 0
127311431 12731143 9 C POWER TO SLEEP PM 2 0
127311431 12731143 11 C RESCUE SLEEP HOMEOPATHICS 1 0
127311431 12731143 13 C CHLORTABS CHLORPHENIRAMINE MALEATE 1 0
127311431 12731143 15 C TURMERIC TURMERIC 1 0
127311431 12731143 17 C PROBIOTICS PROBIOTICS NOS 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127311431 12731143 1 Urinary tract infection

Outcome of event

Event ID CASEID OUTC COD
127311431 12731143 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
127311431 12731143 Arthropathy
127311431 12731143 Fatigue
127311431 12731143 Neuropathy peripheral
127311431 12731143 Pain

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
127311431 12731143 1 20151116 20151124 0