25,729 articles
Pharyngeal reflex
Pharyngeal reflex (gag reflex): involuntary throat contraction protecting the airway, mediated by CN IX afferent and CN X efferent limbs; poorly predictive of dysphagia despite traditional bedside use.
Pharyngeal-cervical-brachial variant of Guillain-Barré syndrome
Pharyngeal-cervical-brachial (PCB) variant of Guillain-Barré syndrome, also called PCB-GBS: a rare localized axonal GBS subtype causing oropharyngeal, neck, and arm weakness with areflexia, linked to anti-GT1a IgG antibodies.
Pharyngectomy
Pharyngectomy: surgical removal of all or part of the pharynx (throat), mainly for throat cancer; ranges from oropharyngectomy to circumferential pharyngolaryngectomy with flap reconstruction.
Pharyngitis
Pharyngitis, inflammation of the pharynx causing sore throat, is mostly viral (about 80% of cases); group A streptococcus causes 20-30% of pediatric and 5-15% of adult cases, diagnosed by Centor criteria, RADT, or throat culture, and treated with penicillin.
Pharyngoplasty
Pharyngoplasty is surgery on the soft palate and pharyngeal walls, with variants that enlarge the velopharynx to treat sleep apnea or narrow it to correct velopharyngeal insufficiency.
Pharyngostomy
Pharyngostomy: surgical creation of an external opening into the pharynx for feeding, drainage, or salivary diversion; an alternative to nasogastric tubes now largely displaced by gastrostomy.
Pharynx
Pharynx (throat): funnel-shaped muscular tube from skull base to C6, shared by digestive and respiratory tracts, divided into nasopharynx, oropharynx, and laryngopharynx; constrictor muscles, vagus and glossopharyngeal innervation, pharyngeal arch embryology.
Phase I/II trial
A Phase I/II trial is a clinical trial design that combines dose escalation and safety evaluation with early evidence of treatment efficacy, aiming to find the optimal biological dose.
Phase II/III trial
A Phase II/III trial, often called a seamless or adaptive seamless design, combines Phase II and Phase III objectives in one protocol, selecting doses at an interim analysis while controlling type I error.
Phase IV trial
A Phase IV trial, also called Phase 4, is a study of a drug after marketing approval, measuring safety, effectiveness, and optimal use in broader patient populations.
Phase-change perfluorocarbon nanodroplets
Phase-change perfluorocarbon nanodroplets (PFCnDs) are submicrometer liquid perfluorocarbon particles that ultrasound or laser light converts into gas microbubbles, enabling on-demand contrast imaging and drug delivery.
Phase-contrast magnetic resonance imaging
Phase-contrast magnetic resonance imaging, also known as phase-contrast MRI, is an MRI technique that measures blood flow noninvasively by encoding fluid velocity into the signal phase.
Phase–amplitude coupling
Phase–amplitude coupling (PAC) is a signal-analysis method quantifying how the amplitude of fast neural oscillations is modulated by the phase of slower ones, used to study cognition and diseases like Parkinson's.
Phases of clinical research
Phases of clinical research: the staged testing of new drugs and health products in humans, from Phase 0 microdosing (10–15 people, <100 micrograms) through Phase I safety (20–100), Phase II dosing, Phase III pivotal trials, to Phase IV post-marketing surveillance.
Phelan-McDermid syndrome
Phelan-McDermid syndrome, or 22q13.3 deletion syndrome, is a rare neurodevelopmental disorder caused by SHANK3 haploinsufficiency, featuring developmental delay, absent speech, hypotonia, and autism spectrum disorder.
Phenacemide
Phenacemide (Phenurone), phenylacetylurea, a 1948 ureide anticonvulsant for refractory psychomotor epilepsy, FDA-approved 1951, withdrawn 2004 due to liver and bone marrow toxicity.
Phenazopyridine
Phenazopyridine (Pyridium, AZO) is an azo-dye urinary analgesic for dysuria, not an antibiotic. Dosed 200 mg three times daily, limited to 2 days; risks include methemoglobinemia and renal or hepatic toxicity.
Phencyclidine
Phencyclidine (PCP, angel dust), 1-(1-phenylcyclohexyl)piperidine, is a dissociative anesthetic and NMDA receptor antagonist synthesized in 1956, abandoned for human use, now a Schedule II drug of abuse.
Phendimetrazine
Phendimetrazine (Bontril PDM, Plegine) is a DEA Schedule III sympathomimetic anorectic, FDA-approved since 1959/1960 for short-term obesity treatment with caloric restriction; 35 mg tablets, tolerance within weeks, over 3 million US prescriptions 2008-2011.
Phenelzine
Phenelzine (Nardil) is an irreversible, nonselective MAO-A/MAO-B inhibitor antidepressant, a hydrazine derivative available since 1960, used mainly for atypical depression, with tyramine dietary restrictions and hypertensive crisis risk.
Phenibut (Фенибут)
Phenibut (Фенибут, fenibut, PhGABA, β-phenyl-γ-aminobutyric acid) is a Russian-developed 1960s GABA_B agonist anxiolytic, not FDA-approved in the US, sold online as a nootropic, with dependence, overdose, and severe withdrawal risks.
Phenicarbazide
Phenicarbazide (1-phenylsemicarbazide, anilinourea, Kryogenin), C7H9N3O, CAS 103-03-7: a phenylhydrazine urea derivative, former INN drug (withdrawn), IARC Group 3, GHS harmful/irritant, found in Heimia plants.
Phenindione
Phenindione is an oral anticoagulant of the indandione class that acts as a vitamin K antagonist, similar to warfarin but now rarely used because of hypersensitivity reactions.
Pheniramine
Pheniramine (pheniramine maleate, Avil) is a first-generation alkylamine H1 antihistamine, FDA approved in 1948, used for allergy, hay fever, colds, motion sickness, and allergic conjunctivitis eye drops; largely supplanted by second-generation antihistamines.
Phenobarbital
Phenobarbital (phenobarbitone, Luminal) is a long-acting barbiturate antiseizure medicine synthesized in 1911, found effective against epilepsy by Hauptmann in 1912, on the WHO essential medicines list since 1977, and a CYP450 enzyme inducer.
Phenotypic screening
Phenotypic screening is a drug discovery method that tests compounds in cells or organisms for observable changes in a disease-relevant phenotype rather than against a pre-specified molecular target.
Phenoxymethylpenicillin
Phenoxymethylpenicillin, or penicillin V, is an acid-stable, narrow-spectrum oral β-lactam antibiotic developed at Lilly from phenoxyacetic acid and made oral by Brandl at Biochemie in 1952; used for streptococcal and respiratory infections.
Phenoxypropazine
Phenoxypropazine (fenoxypropazine, Drazine) is a hydrazine-class, non-selective irreversible MAOI antidepressant marketed by Smith & Nephew from 1961 and withdrawn in 1966 for hepatotoxicity.
Phenprocoumon
Phenprocoumon, sold in Germany as Marcumar since 1953, is a long-acting coumarin oral anticoagulant that inhibits vitamin K epoxide reductase and is used to prevent and treat thrombosis and embolism.
Phensuximide
Phensuximide (Milontin), also called N-methyl-2-phenylsuccinimide, is a succinimide anticonvulsant developed by Parke-Davis in the 1950s for absence (petit mal) seizures; weakly effective, rarely used, and no longer sold in the US.