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
124979052 12497905 2 F 20000602 20160628 20160625 20160707 EXP GB-APOTEX-2016AP009450 APOTEX 0.00 Y 0.00000 20160707 CN GB GB

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
124979052 12497905 1 PS PAROXETINE. PAROXETINE 1 Unknown 20 MG, QD U U 20031 20 MG TABLET
124979052 12497905 2 SS PAROXETINE. PAROXETINE 1 Unknown 20 MG, QD U U 20031 20 MG TABLET
124979052 12497905 3 SS PAROXETINE. PAROXETINE 1 Unknown 20 MG, QD U U 20031 20 MG TABLET
124979052 12497905 4 SS PAROXETINE. PAROXETINE 1 Unknown 20 MG, BID U U 20031 20 MG TABLET BID
124979052 12497905 5 SS PAROXETINE. PAROXETINE 1 Unknown 20 MG, DAILY U U 20031 20 MG TABLET
124979052 12497905 6 SS PAROXETINE. PAROXETINE 1 Unknown 20 MG, BID U U 20031 20 MG TABLET BID
124979052 12497905 7 SS PAROXETINE. PAROXETINE 1 Unknown 20 MG, DAILY U U 20031 20 MG TABLET
124979052 12497905 8 SS PAROXETINE. PAROXETINE 1 Unknown 20 MG, BID U U 20031 20 MG TABLET BID
124979052 12497905 9 SS PAROXETINE. PAROXETINE 1 Unknown 20 MG, QD U U 20031 20 MG TABLET
124979052 12497905 10 SS PAXIL PAROXETINE HYDROCHLORIDE 1 Unknown UNK U U 0 TABLET
124979052 12497905 11 SS PAXIL PAROXETINE HYDROCHLORIDE 1 Unknown 25 MG, QD U U 0 25 MG TABLET
124979052 12497905 12 SS PAXIL PAROXETINE HYDROCHLORIDE 1 Unknown UNK U U 0 TABLET
124979052 12497905 13 SS PAXIL PAROXETINE HYDROCHLORIDE 1 20 MG, QD U U 0 20 MG TABLET
124979052 12497905 14 SS PAXIL PAROXETINE HYDROCHLORIDE 1 Unknown 20 MG, BID U U 0 20 MG TABLET BID
124979052 12497905 15 SS PAXIL PAROXETINE HYDROCHLORIDE 1 Unknown UNK U U 0 TABLET
124979052 12497905 16 C CIPRAMIL /00582602/ CITALOPRAM HYDROBROMIDE 1 Unknown UNK U U 0
124979052 12497905 17 C PROTHIADEN DOTHIEPIN HYDROCHLORIDE 1 Unknown UNK U U 0
124979052 12497905 18 C EFFEXOR VENLAFAXINE HYDROCHLORIDE 1 Unknown UNK U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124979052 12497905 1 Depression
124979052 12497905 10 Panic attack
124979052 12497905 16 Antidepressant therapy
124979052 12497905 17 Product used for unknown indication
124979052 12497905 18 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
124979052 12497905 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124979052 12497905 Agitation
124979052 12497905 Blindness transient
124979052 12497905 Disturbance in attention
124979052 12497905 Dizziness
124979052 12497905 Drug withdrawal syndrome
124979052 12497905 Fatigue
124979052 12497905 Irritability
124979052 12497905 Memory impairment
124979052 12497905 Metamorphopsia
124979052 12497905 Mood swings
124979052 12497905 Nightmare
124979052 12497905 Paraesthesia
124979052 12497905 Weight increased

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
124979052 12497905 1 20160324 0
124979052 12497905 2 20080304 0
124979052 12497905 3 20070831 0
124979052 12497905 4 20060711 0
124979052 12497905 5 200006 0
124979052 12497905 6 19980703 0
124979052 12497905 7 199806 0
124979052 12497905 10 20151022 0
124979052 12497905 11 20150630 0
124979052 12497905 12 20100810 0
124979052 12497905 13 20070831 20100729 0
124979052 12497905 14 20061213 20070730 0
124979052 12497905 15 19980603 20050125 0
124979052 12497905 18 19980601 0