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
126968331 12696833 1 I 20160130 0 20160829 20160829 DIR 52.00 YR F N 140.00000 LBS 20160826 N 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
126968331 12696833 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 Oral 7 TABLET TWICE A DAY N D 0 7 DF COATED TABLET BID
126968331 12696833 3 C METOPROLOL. METOPROLOL 1 0
126968331 12696833 5 C GENERIC K-DUR 2 0
126968331 12696833 7 C LORAZEPAM. LORAZEPAM 1 0
126968331 12696833 9 C MAGNESIUM MAGNESIUM 1 0
126968331 12696833 11 C VITAMIN K PHYTONADIONE 1 0
126968331 12696833 13 C VITAMIN D3 CHOLECALCIFEROL 1 0
126968331 12696833 15 C CALCIUM CALCIUM 1 0
126968331 12696833 17 C PEPCID FAMOTIDINE 1 0
126968331 12696833 19 C ZANTAC RANITIDINE HYDROCHLORIDE 1 0
126968331 12696833 21 C DIGESTIVE ENZYMES UNSPECIFIED INGREDIENT 1 0
126968331 12696833 23 C INOSITOL INOSITOL 1 0
126968331 12696833 25 C D-MANNOSE 2 0
126968331 12696833 27 C FOLIC ACID. FOLIC ACID 1 0
126968331 12696833 29 C FISH OIL FISH OIL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126968331 12696833 1 Urinary tract infection

Outcome of event

Event ID CASEID OUTC COD
126968331 12696833 HO
126968331 12696833 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
126968331 12696833 Abdominal pain upper
126968331 12696833 Amnesia
126968331 12696833 Anxiety
126968331 12696833 Back disorder
126968331 12696833 Bladder disorder
126968331 12696833 Cardiac disorder
126968331 12696833 Decreased appetite
126968331 12696833 Depersonalisation/derealisation disorder
126968331 12696833 Depression
126968331 12696833 Dizziness
126968331 12696833 Dry eye
126968331 12696833 Dry mouth
126968331 12696833 Dyspnoea
126968331 12696833 Dysstasia
126968331 12696833 Feeling abnormal
126968331 12696833 Gait disturbance
126968331 12696833 Gastrointestinal disorder
126968331 12696833 Headache
126968331 12696833 Hyperhidrosis
126968331 12696833 Muscular weakness
126968331 12696833 Nausea
126968331 12696833 Nervous system disorder
126968331 12696833 Nonspecific reaction
126968331 12696833 Pain
126968331 12696833 Panic attack
126968331 12696833 Paraesthesia
126968331 12696833 Pyrexia
126968331 12696833 Renal disorder
126968331 12696833 Syncope
126968331 12696833 Tinnitus
126968331 12696833 Toxicity to various agents
126968331 12696833 Tremor
126968331 12696833 Weight decreased

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
126968331 12696833 1 20151019 20151025 0