Excedrin 250 mg/ 250 mg/ 65 mg film coated tablets Ireland - English - HPRA (Health Products Regulatory Authority)

excedrin 250 mg/ 250 mg/ 65 mg film coated tablets

haleon ireland limited - acetylsalicylic acid; paracetamol; caffeine - film-coated tablet - 250/250/65 milligram(s) - anilides; paracetamol, combinations excl. psycholeptics

Panmigran 250 mg /250 mg /65 mg film-coated tablets Malta - English - Medicines Authority

panmigran 250 mg /250 mg /65 mg film-coated tablets

haleon hellas single member societe anonyme, under the distinctive title of haleon hellas, 274, kifissias ave, 15232 chalandri, athens, greece - film-coated tablet - acetylsalicylic acid 250 mg paracetamol 250 mg caffeine 65 mg - analgesics

MIGRENOL- acetaminophen, caffeine tablet United States - English - NLM (National Library of Medicine)

migrenol- acetaminophen, caffeine tablet

four ventures enterprises, inc. - acetaminophen (unii: 362o9itl9d) (acetaminophen - unii:362o9itl9d), caffeine (unii: 3g6a5w338e) (caffeine - unii:3g6a5w338e) - acetaminophen 500 mg - temporary relief of occasional headaches and minor aches and pains due to  headache, muscular aches, toothache, premenstrual and menstrual cramps pupose: pain reliever, fever reducer

Lopinavir/Ritonavir Mylan European Union - English - EMA (European Medicines Agency)

lopinavir/ritonavir mylan

mylan s.a.s. - lopinavir/ritonavir - hiv infections - antivirals for systemic use, - lopinavir/ritonavir is indicated in combination with other antiretroviral medicinal products for the treatment of human immunodeficiency virus (hiv-1) infected adults, adolescents and children above the age of 2 years.the choice of lopinavir/ritonavir to treat protease inhibitor experienced hiv-1 infected patients should be based on individual viral resistance testing and treatment history of patients.

Efavirenz/Emtricitabine/Tenofovir disoproxil Zentiva European Union - English - EMA (European Medicines Agency)

efavirenz/emtricitabine/tenofovir disoproxil zentiva

zentiva k.s. - efavirenz, emtricitabine, tenofovir disoproxil, phosphate - hiv infections - antivirals for systemic use, - efavirenz/emtricitabine/tenofovir disoproxil zentiva is a fixed-dose combination of efavirenz, emtricitabine and tenofovir disoproxil. it is indicated for the treatment of human immunodeficiency virus-1 (hiv-1) infection in adults aged 18 years and over with virologic suppression to hiv-1 rna levels of < 50 copies/ml on their current combination antiretroviral therapy for more than three months. patients must not have experienced virological failure on any prior antiretroviral therapy and must be known not to have harboured virus strains with mutations conferring significant resistance to any of the three components contained in efavirenz/emtricitabine/tenofovir disoproxil zentiva prior to initiation of their first antiretroviral treatment regimen., the demonstration of the benefit of the combination efavirenz/emtricitabine/tenofovir disoproxil is primarily based on 48-week data from a clinical study in which patients with stable virologic suppression on a combination antiretroviral therapy changed to efavir

LIDOCAINE HYDROCHLORIDE AND DEXTROSE- lidocaine hydrochloride anhydrous and dextrose monohydrate injection, solution United States - English - NLM (National Library of Medicine)

lidocaine hydrochloride and dextrose- lidocaine hydrochloride anhydrous and dextrose monohydrate injection, solution

b. braun medical inc. - lidocaine hydrochloride anhydrous (unii: ec2cnf7xfp) (lidocaine - unii:98pi200987), dextrose monohydrate (unii: lx22yl083g) (anhydrous dextrose - unii:5sl0g7r0ok) - lidocaine hydrochloride anhydrous 0.8 g in 100 ml - lidocaine hydrochloride administered intravenously is specifically indicated in the acute management of (1) ventricular arrhythmias occurring during cardiac manipulations, such as cardiac surgery and (2) life-threatening arrhythmias which are ventricular in origin, such as occur during acute myocardial infarction. lidocaine hydrochloride is contraindicated in patients with a known history of hypersensitivity to local anesthetics of the amide type. lidocaine should not be used in patients with stokes-adams syndrome, wolff-parkinson-white syndrome, or with severe degrees of sinoatrial, atrioventricular, or intraventricular block. solutions containing dextrose may be contraindicated in patients with known allergy to corn or corn products.

LIDOCAINE HYDROCHLORIDE AND DEXTROSE- lidocaine hydrochloride anhydrous and dextrose monohydrate injection, solution United States - English - NLM (National Library of Medicine)

lidocaine hydrochloride and dextrose- lidocaine hydrochloride anhydrous and dextrose monohydrate injection, solution

a-s medication solutions - lidocaine hydrochloride anhydrous (unii: ec2cnf7xfp) (lidocaine - unii:98pi200987), dextrose monohydrate (unii: lx22yl083g) (anhydrous dextrose - unii:5sl0g7r0ok) - lidocaine hydrochloride administered intravenously is specifically indicated in the acute management of (1) ventricular arrhythmias occurring during cardiac manipulations, such as cardiac surgery and (2) life-threatening arrhythmias which are ventricular in origin, such as occur during acute myocardial infarction. lidocaine hydrochloride is contraindicated in patients with a known history of hypersensitivity to local anesthetics of the amide type. lidocaine should not be used in patients with stokes-adams syndrome, wolff-parkinson-white syndrome, or with severe degrees of sinoatrial, atrioventricular, or intraventricular block. solutions containing dextrose may be contraindicated in patients with known allergy to corn or corn products.

LIDOCAINE HCI AND DEXTROSE injection, solution United States - English - NLM (National Library of Medicine)

lidocaine hci and dextrose injection, solution

hf acquisition co llc, dba healthfirst - dextrose monohydrate (unii: lx22yl083g) (anhydrous dextrose - unii:5sl0g7r0ok), lidocaine hydrochloride anhydrous (unii: ec2cnf7xfp) (lidocaine - unii:98pi200987) - lidocaine hydrochloride administered intravenously is specifically indicated in the acute management of (1) ventricular arrhythmias occurring during cardiac manipulations, such as cardiac surgery and (2) life-threatening arrhythmias which are ventricular in origin, such as occur during acute myocardial infarction. lidocaine hydrochloride is contraindicated in patients with a known history of hypersensitivity to local anesthetics of the amide type. lidocaine should not be used in patients with stokes-adams syndrome, wolff-parkinson-white syndrome, or with severe degrees of sinoatrial, atrioventricular, or intraventricular block. solutions containing dextrose may be contraindicated in patients with known allergy to corn or corn products.

LIDOCAINE HYDROCHLORIDE AND DEXTROSE- lidocaine hydrochloride anhydrous and dextrose monohydrate injection, solution United States - English - NLM (National Library of Medicine)

lidocaine hydrochloride and dextrose- lidocaine hydrochloride anhydrous and dextrose monohydrate injection, solution

a-s medication solutions - lidocaine hydrochloride (unii: v13007z41a) (lidocaine - unii:98pi200987), dextrose monohydrate (unii: lx22yl083g) (anhydrous dextrose - unii:5sl0g7r0ok) - lidocaine hydrochloride administered intravenously is specifically indicated in the acute management of (1) ventricular arrhythmias occurring during cardiac manipulations, such as cardiac surgery and (2) life-threatening arrhythmias which are ventricular in origin, such as occur during acute myocardial infarction. lidocaine hydrochloride is contraindicated in patients with a known history of hypersensitivity to local anesthetics of the amide type. lidocaine should not be used in patients with stokes-adams syndrome, wolff-parkinson-white syndrome, or with severe degrees of sinoatrial, atrioventricular, or intraventricular block. solutions containing dextrose may be contraindicated in patients with known allergy to corn or corn products.