Adverse Drug Reaction Reporting Form Reporter InformationPatient InformationDrug InformationAdverse Event DetailsMedical History Reporter NamePhone NumberAddressCity/Governorate CountrySelect CountryAfghanistanAland IslandsAlbaniaAlgeriaAmerican SamoaAndorraAngolaAnguillaAntarcticaAntigua and BarbudaArgentinaArmeniaArubaAustraliaAustriaAzerbaijanBahamasBahrainBangladeshBarbadosBelarusBelgiumBelizeBeninBermudaBhutanBoliviaBonaire, Saint Eustatius and SabaBosnia and HerzegovinaBotswanaBouvet IslandBrazilBritish Indian Ocean TerritoryBritish Virgin IslandsBruneiBulgariaBurkina FasoBurundiCabo VerdeCambodiaCameroonCanadaCayman IslandsCentral African RepublicChadChileChinaChristmas IslandCocos (Keeling) IslandsColombiaComorosCook IslandsCosta RicaCroatiaCubaCuraçaoCyprusCzech RepublicDemocratic Republic of the Congo (Kinshasa)DenmarkDjiboutiDominicaDominican RepublicEcuadorEgyptEl SalvadorEquatorial GuineaEritreaEstoniaEswatiniEthiopiaFalkland IslandsFaroe IslandsFijiFinlandFranceFrench GuianaFrench PolynesiaFrench Southern TerritoriesGabonGambiaGeorgiaGermanyGhanaGibraltarGreeceGreenlandGrenadaGuadeloupeGuamGuatemalaGuernseyGuineaGuinea-BissauGuyanaHaitiHeard Island and McDonald IslandsHondurasHong KongHungaryIcelandIndiaIndonesiaIranIraqIrelandIsle of ManIsraelItalyIvory CoastJamaicaJapanJerseyJordanKazakhstanKenyaKiribatiKosovoKuwaitKyrgyzstanLaosLatviaLebanonLesothoLiberiaLibyaLiechtensteinLithuaniaLuxembourgMacao S.A.R., ChinaMadagascarMalawiMalaysiaMaldivesMaliMaltaMarshall IslandsMartiniqueMauritaniaMauritiusMayotteMexicoMicronesiaMoldovaMonacoMongoliaMontenegroMontserratMoroccoMozambiqueMyanmarNamibiaNauruNepalNetherlandsNew CaledoniaNew ZealandNicaraguaNigerNigeriaNiueNorfolk IslandNorth KoreaNorth MacedoniaNorthern Mariana IslandsNorwayOmanPakistanPalauPalestinian TerritoryPanamaPapua New GuineaParaguayPeruPhilippinesPitcairnPolandPortugalPuerto RicoQatarRepublic of the Congo (Brazzaville)RomaniaRussiaRwandaRéunionSaint BarthélemySaint HelenaSaint Kitts and NevisSaint LuciaSaint Martin (Dutch part)Saint Martin (French part)Saint Pierre and MiquelonSaint Vincent and the GrenadinesSamoaSan MarinoSao Tome and PrincipeSaudi ArabiaSenegalSerbiaSeychellesSierra LeoneSingaporeSlovakiaSloveniaSolomon IslandsSomaliaSouth AfricaSouth Georgia/Sandwich IslandsSouth KoreaSouth SudanSpainSri LankaSudanSurinameSvalbard and Jan MayenSwedenSwitzerlandSyriaTaiwanTajikistanTanzaniaThailandTimor-LesteTogoTokelauTongaTrinidad and TobagoTunisiaTurkmenistanTurks and Caicos IslandsTuvaluTürkiyeUgandaUkraineUnited Arab EmiratesUnited Kingdom (UK)United States (US)United States (US) Minor Outlying IslandsUnited States (US) Virgin IslandsUruguayUzbekistanVanuatuVaticanVenezuelaVietnamWallis and FutunaWestern SaharaYemenZambiaZimbabweReporter Patient Relationship Physician Pharmacist Nurse Patient Patient's relative/Caregiver OtherPreviousNextPatient IntialsGender Male FemaleAge (Year)Select an Age Group Children (0-14) years Youth (15-24) years Young Adults (25-44) years Middle Age (45-59) years Elderly (60-74) years Senior (+75) yearsWeight (Kg) PreviousNextProduct NamePlease Select Product NameCitrivolDesfaxinateDiabentaEjadaxtinFloxatavSchisolazineTecentacavVomifratonWadigabalinZemmuneWadizidovActive Product Ingredient (s) Strength (Concentration)Dosage / Pharmaceutical FormDoseRoute of Administration Oral Injection Topical Inhalation OtherOther (Please specify)Start DateDate Stopped (If applicable)PreviousNextDescribe reactionDate of Reaction StartedCheck all appropriate to adverse reaction Patient died Involved or prolonged inpatient hospitalization Involved persistence/significance/ disability or incapacity Life threatening Congenital anomaly Other medically important condition Non-seriousReaction Outcome Recovered Recovering Not recovered Fatal Recovered with sequelae UnknownDate of RecoveryWas the drug discontinued? Unknown Yes No OtherOtherDid reaction abate after stopping drug? Yes No N/ADid reaction reappear after reintroduction? Yes No Effect unknown N/APreviousNextRelevant Medical HistoryOther relevant History, including pre-existing medical conditions (e.g. allergies, pregnancy, smoking, hepatic / renal dysfunction etc):Relevant medication History & Concomitant Drug (please list any other drugs taken during the last month prior to the reaction) Previous Submit Form
