Medicines
Every medicine on MedUnfold traces back to official sources.
176 medicines published
Cancer
44CDK4/6 inhibitor3
Verzenio (abemaciclib) is an oral CDK4/6 inhibitor from Eli Lilly. It blocks cyclin-dependent kinases 4 and 6, keeps the retinoblastoma (Rb) protein unphosphorylated, and arrests cancer cells in the G1 phase before they can replicate their DNA. It is used, mostly alongside endocrine therapy, in hormone receptor-positive, HER2-negative breast cancer.
Ibrance (palbociclib) is an oral CDK4/6 inhibitor from Pfizer for hormone receptor-positive, HER2-negative advanced or metastatic breast cancer. Combined with endocrine therapy, it blocks the cell-cycle machinery cancer cells use to multiply, slowing or stopping tumour growth.
Kisqali (ribociclib) is an oral CDK4/6 inhibitor from Novartis for hormone receptor-positive, HER2-negative breast cancer. With endocrine therapy it is used for high-risk early breast cancer after surgery and for advanced or metastatic disease, blocking the cell-cycle machinery cancer cells use to multiply.
BTK inhibitor2
Calquence (acalabrutinib) is a selective Bruton tyrosine kinase (BTK) inhibitor from AstraZeneca. By locking BTK, it cuts the survival and multiplication signal that malignant B cells rely on, and is used in chronic lymphocytic leukaemia and mantle cell lymphoma, alone or with antibody-based combinations.
Imbruvica (ibrutinib) is the first-in-class Bruton tyrosine kinase inhibitor. Taken by mouth, it blocks the survival signalling of malignant B cells and transformed the treatment of chronic lymphocytic leukaemia, Waldenstrom macroglobulinaemia and mantle cell lymphoma.
VEGF inhibitor2
Eylea (aflibercept) is a VEGF inhibitor from Bayer that acts as a decoy receptor, trapping vascular endothelial growth factor before it can stimulate abnormal blood vessel growth in the retina. It is injected into the eye to treat neovascular age-related macular degeneration, diabetic macular oedema, macular oedema after retinal vein occlusion, diabetic retinopathy, and retinopathy of prematurity.
Avastin (bevacizumab) is a humanised antibody from Roche that binds vascular endothelial growth factor (VEGF). By starving tumours of new blood vessels it slows their growth, and is used with chemotherapy in several advanced cancers, including colorectal and lung cancer.
ALK tyrosine kinase inhibitor1
androgen receptor inhibitor3
Erleada (apalutamide) is an oral androgen receptor inhibitor from Janssen for prostate cancer. It blocks the receptor that prostate tumour cells need to grow, and is used in non-metastatic castration-resistant disease and, with androgen deprivation therapy, in metastatic hormone-sensitive disease.
Nubeqa (darolutamide) is an androgen receptor inhibitor from Bayer for prostate cancer. It blocks the receptor that drives tumour growth and is used in non-metastatic castration-resistant disease and, with androgen deprivation therapy, in metastatic hormone-sensitive disease.
Xtandi (enzalutamide) is an androgen receptor inhibitor from Astellas for prostate cancer. It blocks androgen binding, receptor activation and nuclear signalling in one drug, and is used across castration-resistant and hormone-sensitive disease settings.
PD-L1 checkpoint inhibitor3
Tecentriq (atezolizumab) is a PD-L1 checkpoint inhibitor from Genentech. By releasing the brake that tumours put on immune T cells, it lets the immune system attack cancer, and is used in selected lung cancers, urothelial carcinoma and other settings defined by PD-L1 testing.
Imfinzi (durvalumab) is a PD-L1 checkpoint inhibitor from AstraZeneca. By lifting the PD-L1 brake on T cells it restores immune attack on cancer, and is used around surgery in resectable lung cancer and after chemoradiation or chemotherapy in other lung cancer settings.
Cejemly (sugemalimab) is a PD-L1 checkpoint inhibitor from CStone Pharmaceuticals approved in the European Union for non-small cell lung cancer. With platinum-based chemotherapy it is a first-line treatment of metastatic disease, and as monotherapy it treats unresectable stage III disease after chemoradiotherapy.
multi-kinase inhibitor2
Cabozantinib is an oral multi-kinase inhibitor that blocks MET, VEGF receptors and RET, pathways tumours use to grow and build blood supply. As Cabometyx it is used in advanced kidney and liver cancer and thyroid cancer; as Cometriq, in medullary thyroid carcinoma.
Lenvima (lenvatinib) is an oral multi-kinase inhibitor from Eisai that blocks VEGF and FGF receptors driving tumour blood supply. It is used in radioactive iodine-refractory thyroid cancer, advanced kidney cancer and, with pembrolizumab, in endometrial cancer.
PD-1 checkpoint inhibitor9
Libtayo (cemiplimab) is a PD-1 checkpoint inhibitor from Regeneron. By releasing exhausted T cells from the PD-1 brake, it restores immune attack on cancer cells and is used in advanced skin cancers and, with chemotherapy, in non-small cell lung cancer.
Jemperli (dostarlimab) is a PD-1 checkpoint inhibitor from GlaxoSmithKline. It reawakens T cells against mismatch repair-deficient cancers and is used in advanced endometrial cancer, alone or with chemotherapy, and in selected previously treated solid tumours.
Opdivo (nivolumab) is a PD-1 checkpoint inhibitor from Bristol-Myers Squibb used across many cancers, including melanoma, lung, kidney, bladder, liver, esophageal and gastric cancers, and Hodgkin lymphoma. By releasing the PD-1 brake on T cells, it restores immune attack on tumours, alone or with combinations.
Keytruda (pembrolizumab) is a PD-1 checkpoint inhibitor from Merck used across many cancers, including melanoma, lung, kidney, gastric, and triple-negative breast cancers, Hodgkin lymphoma, and MSI-H or dMMR tumours. By releasing the PD-1 brake on T cells, it restores immune attack on cancer, alone or with combinations.
Penpulimab-kcqx is a PD-1 checkpoint inhibitor from Akeso Biopharma for non-keratinizing nasopharyngeal carcinoma. It is used with platinum chemotherapy plus gemcitabine as first-line treatment of recurrent or metastatic disease, and alone after platinum-based chemotherapy and at least one later line of therapy.
Zynyz (retifanlimab) is a PD-1 checkpoint inhibitor from Incyte for two rare cancers. With carboplatin and paclitaxel it is a first-line treatment for advanced squamous cell carcinoma of the anal canal, and as monotherapy it treats metastatic or locally advanced Merkel cell carcinoma.
Hetronifly (serplulimab) is a PD-1 checkpoint inhibitor from Accord Healthcare used in the European Union with chemotherapy as first-line treatment for extensive-stage small cell lung cancer, non-squamous non-small cell lung cancer without EGFR, ALK, or ROS1 mutations, and PD-L1-positive esophageal squamous cell carcinoma.
Tevimbra (tislelizumab) is a PD-1 checkpoint inhibitor from BeOne Medicines for esophageal squamous cell carcinoma, gastric and gastroesophageal junction adenocarcinoma, and non-small cell lung cancer. By releasing the PD-1 brake on T cells, it restores immune attack on tumours, alone or with chemotherapy.
Loqtorzi (toripalimab) is a PD-1 checkpoint inhibitor from Coherus Oncology for nasopharyngeal carcinoma. With cisplatin and gemcitabine it is a first-line treatment of metastatic or recurrent locally advanced disease, and as monotherapy it treats disease that has progressed after platinum chemotherapy.
EGFR-blocking antibody1
BRAF kinase inhibitor1
CD38-directed antibody1
selective estrogen receptor degrader (SERD)1
VEGFR kinase inhibitor1
tyrosine kinase inhibitor1
CTLA-4 checkpoint inhibitor1
CD38-directed cytolytic antibody1
IDH1 inhibitor1
immunomodulatory imide drug1
PARP inhibitor2
Zejula (niraparib) is an oral PARP inhibitor from GlaxoSmithKline used as maintenance treatment for advanced ovarian, fallopian tube, or primary peritoneal cancer that has responded to platinum-based chemotherapy. It blocks DNA repair enzymes cancer cells depend on, so DNA damage accumulates and the cells die.
Lynparza (olaparib) is an oral PARP inhibitor from AstraZeneca for selected BRCA-mutated or homologous recombination-deficient cancers of the ovary, breast, pancreas, and prostate. It blocks DNA repair enzymes that cancer cells depend on, so damaged cancer cells die while treatment helps keep responding cancers from returning.
third-generation EGFR tyrosine kinase inhibitor1
HER2/neu receptor antagonist2
Perjeta (pertuzumab) is a HER2/neu receptor antagonist from Genentech that blocks HER2 from pairing with other HER family receptors, shutting down a key growth signal in HER2-positive breast cancer. It is used with trastuzumab and chemotherapy in metastatic, neoadjuvant, and adjuvant settings.
Herceptin (trastuzumab) is a humanized monoclonal antibody from Roche that targets the HER2 receptor on cancer cells. It treats HER2-overexpressing breast cancer in early and metastatic settings and HER2-overexpressing metastatic gastric or gastroesophageal junction adenocarcinoma, with patients selected by companion diagnostic testing.
BCR-ABL tyrosine kinase inhibitor1
CD20-directed monoclonal antibody1
BCL-2 inhibitor1
Bruton's tyrosine kinase (BTK) inhibitor1
Immune & inflammation
23TNF-alpha inhibitor3
Humira (adalimumab) is a fully human monoclonal antibody from AbbVie that neutralises tumour necrosis factor alpha (TNF-alpha), a key driver of inflammatory disease. It is used across several chronic inflammatory conditions, including rheumatoid arthritis, Crohn disease, ulcerative colitis, plaque psoriasis and uveitis.
Cimzia (certolizumab pegol) is a PEGylated antibody fragment from UCB that neutralises TNF-alpha. Without the Fc portion, it is designed to calm inflammation in rheumatoid arthritis and Crohn disease while behaving differently from full-length antibodies.
Remicade (infliximab) is a chimeric antibody that binds and neutralises TNF-alpha, one of the first biologics for inflammatory disease. Given by infusion, it is used in Crohn disease, ulcerative colitis, rheumatoid arthritis and other immune conditions.
JAK inhibitor2
Olumiant (baricitinib) is an oral Janus kinase inhibitor from Eli Lilly. By damping JAK-STAT signalling it reduces inflammatory cytokine activity, and is used in rheumatoid arthritis after TNF blockers, in hospitalized adults with severe COVID-19, and in severe alopecia areata.
Rinvoq (upadacitinib) is an oral Janus kinase (JAK) inhibitor from AbbVie for several immune-mediated inflammatory diseases, including rheumatoid arthritis, psoriatic arthritis, axial spondyloarthritis, atopic dermatitis, giant cell arteritis, ulcerative colitis, and Crohn's disease, usually after an inadequate response to prior therapy such as TNF blockers or DMARDs.
interleukin-5 receptor alpha-directed cytolytic monoclonal antibody1
IL-17A and IL-17F inhibitor1
targeted-release corticosteroid1
IL-4/IL-13 signalling inhibitor1
TNF blocker1
IL-23 inhibitor3
Tremfya (guselkumab) is a monoclonal antibody from Janssen that selectively blocks interleukin-23, a driver of psoriatic inflammation. It clears skin in plaque psoriasis and treats psoriatic arthritis, in adults and children from six years.
Skyrizi (risankizumab) is an interleukin-23 inhibitor from AbbVie for moderate to severe plaque psoriasis, active psoriatic arthritis, and moderately to severely active Crohn's disease and ulcerative colitis. It calms the IL-23-driven inflammatory loop behind these conditions.
Ilumya (tildrakizumab) is an interleukin-23 inhibitor for adults with moderate to severe plaque psoriasis who are candidates for systemic therapy or phototherapy. Given by injection at spaced intervals, it calms the IL-23-driven inflammatory loop behind psoriatic plaques.
IL-17A inhibitor2
Taltz (ixekizumab) is an interleukin-17A inhibitor from Eli Lilly that neutralises a key cytokine driving inflammation in skin, joints, and spine. It treats moderate-to-severe plaque psoriasis, psoriatic arthritis, ankylosing spondylitis, and non-radiographic axial spondyloarthritis in adults.
Cosentyx (secukinumab) is an interleukin-17A inhibitor from Novartis for plaque psoriasis, psoriatic arthritis, ankylosing spondylitis, non-radiographic axial spondyloarthritis, enthesitis-related arthritis, and hidradenitis suppurativa. It blocks a key cytokine that sustains inflammation in skin, joints, and spine.
IL-13 inhibitor2
Ebglyss (lebrikizumab) is a monoclonal antibody from Eli Lilly that selectively neutralises interleukin-13, a key driver of type 2 inflammation in atopic dermatitis. It is used in moderate-to-severe disease in adults and adolescents when topical treatment is not enough.
Adbry (tralokinumab) is an interleukin-13 antagonist from LEO Pharma for moderate to severe atopic dermatitis in patients aged 12 years and older whose disease is not adequately controlled with topical prescription therapies. It can be used with or without topical corticosteroids.
IL-5 antagonist1
Janus kinase (JAK) inhibitor2
Jakafi (ruxolitinib) is a Janus kinase inhibitor from Incyte that blocks JAK1 and JAK2, calming overactive immune and blood-cell signalling. It treats myelofibrosis, polycythaemia vera, and both acute and chronic graft-versus-host disease when other therapies have not worked.
Xeljanz (tofacitinib) is an oral Janus kinase inhibitor from Pfizer that calms overactive immune signalling. After TNF blockers have not worked, it treats rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis, ulcerative colitis, and certain childhood arthritis forms.
IL-6 receptor antagonist1
IL-12 and IL-23 inhibitor1
integrin receptor antagonist1
Metabolic & hormonal
16alpha-glucosidase inhibitor1
SGLT2 inhibitor3
Invokana (canagliflozin) is an SGLT2 inhibitor from Janssen. It makes the kidneys excrete extra glucose, lowering blood sugar in type 2 diabetes, and it also reduces major cardiovascular events and diabetic kidney disease progression in at-risk adults.
Farxiga (dapagliflozin) is an SGLT2 inhibitor from AstraZeneca. It makes the kidneys excrete extra glucose, lowering blood sugar in type 2 diabetes, and it also protects against heart failure hospitalisation in people with diabetes and cardiovascular risk.
Jardiance (empagliflozin) is an SGLT2 inhibitor from Boehringer Ingelheim. It lowers blood sugar by letting glucose leave through the urine, and it also protects the heart and kidneys, reducing heart failure hospitalisation and kidney disease progression.
GLP-1 receptor agonist3
Trulicity (dulaglutide) is a once-weekly GLP-1 receptor agonist from Eli Lilly for type 2 diabetes. It boosts insulin when glucose is high, calms glucagon and slows stomach emptying, improving blood sugar and reducing major cardiovascular events in at-risk adults.
Victoza (liraglutide) is a once-daily GLP-1 receptor agonist from Novo Nordisk for type 2 diabetes. A fatty acid tail keeps it in the blood for about a day, boosting meal-time insulin, calming glucagon and slowing stomach emptying to lower blood sugar.
Ozempic (semaglutide) is a GLP-1 receptor agonist from Novo Nordisk for adults with type 2 diabetes. Alongside diet and exercise it improves blood sugar control, reduces major cardiovascular events in people with established cardiovascular disease, and protects kidney function in chronic kidney disease.
progestin contraceptive1
rapid-acting insulin analogue2
NovoLog (insulin aspart) is a rapid-acting insulin from Novo Nordisk. A single amino acid change makes it absorb quickly after injection, so it covers the rise in blood sugar that follows a meal, and it is used in type 1 and type 2 diabetes.
Humalog (insulin lispro) is a rapid-acting insulin from Eli Lilly. Two swapped amino acids make it absorb quickly after injection, so it covers the rise in blood sugar that follows a meal, and it is used in type 1 and type 2 diabetes.
long-acting insulin analogue2
Tresiba (insulin degludec) is an ultra-long-acting basal insulin from Novo Nordisk. After injection it forms multi-hexamer chains under the skin that release insulin steadily for more than 24 hours, providing a stable, peakless background level for diabetes control.
Lantus (insulin glargine) is a long-acting basal insulin from Sanofi. A single daily injection provides a steady, peakless insulin level for about 24 hours, controlling blood sugar in type 1 diabetes and in type 2 diabetes when other medicines are not enough.
biguanide1
cortisol synthesis inhibitor1
DPP-4 inhibitor1
dual GIP and GLP-1 receptor agonist1
Heart & blood
18recombinant coagulation factor IX1
PCSK9 inhibitor2
Praluent (alirocumab) is a PCSK9 inhibitor from Sanofi and Regeneron. By blocking PCSK9, it preserves LDL receptors on liver cells, sharply lowering LDL cholesterol and reducing major cardiovascular events in adults at increased risk.
Repatha (evolocumab) is a PCSK9 inhibitor from Amgen. By protecting LDL receptors from destruction, it dramatically lowers LDL cholesterol and reduces major cardiovascular events in adults at increased risk.
calcium channel blocker1
factor Xa inhibitor3
Eliquis (apixaban) is an oral factor Xa inhibitor from Bristol-Myers Squibb and Pfizer. By interrupting one key step of the clotting cascade it prevents harmful clots, and is used to reduce stroke risk in atrial fibrillation and to treat and prevent deep vein thrombosis and pulmonary embolism.
Savaysa (edoxaban) is an oral factor Xa inhibitor from Daiichi Sankyo. By blocking one central step of the clotting cascade it reduces stroke risk in atrial fibrillation and treats deep vein thrombosis and pulmonary embolism after initial injectable therapy.
Xarelto (rivaroxaban) is an oral factor Xa inhibitor from Bayer that blocks a key enzyme of the clotting cascade. It prevents and treats deep vein thrombosis and pulmonary embolism, reduces stroke risk in atrial fibrillation, and lowers cardiovascular events after acute coronary syndromes or in coronary and peripheral artery disease.
salicylate anti-inflammatory1
HMG-CoA reductase inhibitor (statin)2
Lipitor (atorvastatin) is a statin that lowers LDL cholesterol by slowing its production in the liver and helping clear it from the blood. Beyond lowering numbers, it reduces the risk of heart attack and stroke in people with cardiovascular risk factors or established heart disease.
Crestor (rosuvastatin) is a statin that lowers LDL cholesterol by slowing its production in the liver. As an adjunct to diet it treats high cholesterol, familial hypercholesterolemia, and certain triglyceride disorders, and it reduces the risk of major cardiovascular events in people at increased risk.
P2Y12 platelet inhibitor2
Plavix (clopidogrel) is a P2Y12 platelet inhibitor from Sanofi that prevents platelets from clumping into clots. It reduces the risk of heart attack and stroke after acute coronary syndromes, recent myocardial infarction, recent stroke, or established peripheral arterial disease.
Brilinta (ticagrelor) is a P2Y12 platelet inhibitor from AstraZeneca that prevents platelets from clumping into clots. It reduces heart attack and stroke risk in high-risk coronary artery disease and after acute coronary syndromes or myocardial infarction, and lowers stroke risk after minor ischemic stroke or high-risk TIA.
direct thrombin inhibitor1
long-acting G-CSF analogue1
ACE inhibitor1
angiotensin receptor-neprilysin inhibitor1
transthyretin stabilizer (ATTR cardiomyopathy)1
prostacyclin mimetic1
Infections & vaccines
12penicillin antibiotic1
integrase strand transfer inhibitor3
Biktarvy combines bictegravir with emtricitabine and tenofovir alafenamide into a single daily tablet from Gilead for HIV-1 infection. Bictegravir blocks the viral integrase enzyme, stopping HIV from inserting its genetic material into infected cells.
Apretude (cabotegravir) is a long-acting injectable integrase inhibitor from ViiV Healthcare used for pre-exposure prophylaxis (PrEP) to reduce the risk of sexually acquired HIV-1 infection in adults and adolescents at risk. Given as an intramuscular injection every two months after the initial doses, it keeps protective drug levels in the body between shots.
Tivicay (dolutegravir) is an integrase inhibitor from ViiV Healthcare for HIV-1 infection, always used with other antiretrovirals. It blocks the viral integrase enzyme so HIV cannot splice its genes into infected cells, keeping viral levels suppressed.
cephalosporin antibiotic1
first-generation cephalosporin antibiotic1
mRNA COVID-19 vaccine1
integrase strand transfer inhibitor and nucleoside analogue reverse transcriptase inhibitor combination1
HPV vaccine1
HIV-1 capsid inhibitor1
pneumococcal conjugate vaccine1
recombinant zoster vaccine1
Brain & mind
17atypical antipsychotic6
Abilify (aripiprazole) is an atypical antipsychotic from Otsuka. Rather than fully blocking dopamine signals, it partially stimulates dopamine D2 receptors, steadying overactive circuits. It is used in schizophrenia and bipolar I disorder, and as add-on therapy in major depressive disorder.
Rexulti (brexpiprazole) is an atypical antipsychotic from Otsuka that modulates dopamine and serotonin receptors. It is used in schizophrenia, as an add-on to antidepressants in major depressive disorder, and for agitation associated with dementia due to Alzheimer's disease.
Vraylar (cariprazine) is an atypical antipsychotic with a unique preference for dopamine D3 receptors. It is used for schizophrenia, manic or mixed episodes of bipolar I disorder, bipolar depression, and as add-on therapy for major depressive disorder. Rather than fully blocking dopamine signals, it partially stimulates D3 and D2 receptors, helping to stabilize overactive circuits.
Latuda (lurasidone) is an atypical antipsychotic that modulates dopamine and serotonin receptors. It treats schizophrenia in adults and adolescents, and depressive episodes of bipolar I disorder, alone or with mood stabilisers.
Invega (paliperidone) is an atypical antipsychotic used for schizophrenia and schizoaffective disorder. It blocks dopamine D2 and serotonin 5-HT2A receptors, calming overactive signaling in thought and mood circuits. It is the major active metabolite of risperidone and is formulated as a once-daily extended-release tablet.
Seroquel (quetiapine) is an atypical antipsychotic used for schizophrenia, manic and depressive episodes of bipolar I disorder, and as add-on treatment in major depressive disorder. It modulates dopamine and serotonin receptors, calming overactive signaling in mood and thought circuits.
anticonvulsant1
CGRP receptor antagonist2
Aimovig (erenumab) is a monoclonal antibody from Amgen that blocks the receptor for calcitonin gene-related peptide (CGRP), a key signaling molecule in migraine. Given once monthly by injection, it prevents migraine attacks in adults.
Nurtec ODT (rimegepant) is a small-molecule CGRP receptor antagonist (a "gepant") from Pfizer. Taken as an orally disintegrating tablet, it both treats acute migraine attacks and, on an every-other-day schedule, prevents episodic migraine in adults.
CGRP antagonist2
Ajovy (fremanezumab) is a monoclonal antibody from Teva that binds calcitonin gene-related peptide (CGRP), a key molecule in migraine biology. Given monthly or quarterly by injection, it prevents migraine attacks in adults and selected adolescents.
Emgality (galcanezumab) is a monoclonal antibody from Eli Lilly that binds and neutralizes calcitonin gene-related peptide (CGRP), a key signaling molecule in migraine. Given once monthly by injection, it prevents migraine in adults and treats episodic cluster headache.
α4-integrin antibody (multiple sclerosis)1
antisense oligonucleotide (spinal muscular atrophy)1
CD20-directed monoclonal antibody (multiple sclerosis)1
gabapentinoid anticonvulsant1
intravenous general anesthetic1
VMAT2 inhibitor1
Breathing & allergy
4inhaled corticosteroid and long-acting beta-2 agonist combination1
long-acting beta-2 agonist1
antihistamine and corticosteroid nasal spray1
short-acting beta2-adrenergic agonist1
Eye care
2prostaglandin analog2
Zioptan (tafluprost) is a prostaglandin analog eye drop from Thea Pharma. Used once daily, it lowers elevated intraocular pressure in patients with open-angle glaucoma or ocular hypertension by helping fluid drain from the eye.
Travatan (travoprost) is a prostaglandin analogue eye drop from Novartis that lowers raised intraocular pressure. In the European Union it is used in adults with ocular hypertension or open-angle glaucoma, and in children from 2 months of age with ocular hypertension or paediatric glaucoma.
Other areas
40selective T-cell costimulation modulator1
CYP17 inhibitor1
topical retinoid1
phosphodiesterase 4 (PDE4) inhibitor1
macrolide antibacterial1
cap-dependent endonuclease inhibitor1
FGF23-blocking antibody1
proteasome inhibitor1
COX-2 selective nonsteroidal anti-inflammatory drug1
RANKL inhibitor1
vasopressin analogue1
TYK2 inhibitor1
acetylcholinesterase inhibitor1
serotonin–norepinephrine reuptake inhibitor1
CFTR modulator combination1
nucleoside and nucleotide reverse transcriptase inhibitor combination1
Nectin-4-directed antibody-drug conjugate1
selective serotonin reuptake inhibitor2
Lexapro (escitalopram) is a selective serotonin reuptake inhibitor used for major depressive disorder and generalized anxiety disorder. It blocks the serotonin transporter, leaving more serotonin available in the synapse to help restore mood balance. It is one of the most selective SSRIs available.
Zoloft (sertraline) is a selective serotonin reuptake inhibitor used for depression, obsessive-compulsive disorder, panic disorder, PTSD, social anxiety disorder, and premenstrual dysphoric disorder. It blocks the serotonin transporter, increasing serotonin signaling in mood and fear circuits. It is one of the most widely prescribed antidepressants.
cholesterol absorption inhibitor1
immune globulin (intravenous/subcutaneous)1
fluoroquinolone antibacterial1
NMDA receptor antagonist1
leukotriene receptor antagonist1
anti-IgE monoclonal antibody1
proton pump inhibitor2
Omeprazole (Prilosec) is a proton pump inhibitor that reduces the amount of acid the stomach makes. It treats frequent heartburn over the counter, and by prescription it is used for gastroesophageal reflux disease, acid-related ulcers, and conditions with excess stomach acid.
Pantoprazole (Protonix) is a proton pump inhibitor that reduces the amount of acid the stomach makes. It heals erosive esophagitis from gastroesophageal reflux disease, keeps it healed, treats excess acid conditions such as Zollinger-Ellison syndrome, and relieves reflux symptoms.
neuraminidase inhibitor1
CD79b-directed antibody-drug conjugate1
sclerostin inhibitor1
Trop-2-directed antibody-drug conjugate1
PDE5 inhibitor2
Viagra (sildenafil) is a PDE5 inhibitor originally from Pfizer. By blocking the enzyme that breaks down cGMP, it enhances blood flow to the penis during sexual stimulation, treating erectile dysfunction; a separate formulation (Revatio) treats pulmonary arterial hypertension.
Cialis (tadalafil) is a PDE5 inhibitor from Eli Lilly. By blocking the enzyme that breaks down cGMP, it enhances blood flow to the penis during sexual stimulation for erectile dysfunction, and it also relaxes smooth muscle in the prostate and bladder to relieve symptoms of benign prostatic hyperplasia.