MOA of drugs
Quiz yourself by thinking what should be in
each of the black spaces below before clicking
on it to display the answer.
Help!
|
|
||||
---|---|---|---|---|---|
Competitive blockers (SM Relaxants) | Prevent ACh from binding to the NMJ and prevent depolarisation
🗑
|
||||
Persistent depolarisers (SM Relaxants) | ACh analogues binding to NMJ and depolarise for a longer time
🗑
|
||||
DIRECTLY ACTING MUSCLE RELAXANTS | PREVENT CALCIUM ION CHANNEL
🗑
|
||||
MEPHENESIN | INHIBIT POLYSYNAPTIC REFLEXES
🗑
|
||||
BENZODIAZEPINE | INCREASE GABA CHANNELS
🗑
|
||||
GABA DERIVATIVE | INCREASES GABA ACTION
🗑
|
||||
CENTRAL ALPHA-2 AGONIST | PRESYNAPTIC INHIBITION WHICH INHIBITS RELEASE OF EXCITATORY AMINO ACIDS
🗑
|
||||
QUININE | DECREASES THE EXCITABILITY OF THE NMJ
🗑
|
||||
BOTULINUM | PREVENTS CALCIUM DEPENDENT ACh RELEASE
🗑
|
||||
LOCAL ANAESTHETICS | BLOCK Na CHANNELS
🗑
|
||||
THIAZIDE DIURETICS | REDUCE REABSORPTION OF Na AND WATER IN THE PROXIMAL PART OF DISTAL TUBULE
🗑
|
||||
LOOP DIURETICS | REDUCE REABSORPTION IN LIMB OF LOOP OF HENLE
🗑
|
||||
POTASSIUM SPARING DIURETICS | REDUCE REABSORPTION OF Na AT THE DISTAL PART OF THE DISTAL TUBULE AND ALSO REDUCE K EXCRETION
🗑
|
||||
ALDOSTERONE RECEPTOR ANTAG | REDUCE ALDOSTERONE IN ORDER TO PREVENT Na AND WATER REABSORPTION IN DT AND CT
🗑
|
||||
OSMOTIC DIURETICS | INCREASE THE OSMOLARITY OF THE FILTRATE AND INCREASES THE FILTRATION LOAD AND REDUCES REABSORPTION . DUE TO HIGH OSMOTIC PRESSURE ADH IS ALSO INEFFECTIVE
🗑
|
||||
CA INHIBITORS | PREVENT THE ENZYME FEOM ACTING AND HENCE PREVENT Na AND WATER REABSORPTION
🗑
|
||||
XANTHINES | DILATES AFFERENT ARTERIOLES and prevents reabsorption of water and Na
🗑
|
||||
VASOPRESSIN | INCREASES REABSORPTION OF Na AND WATER
🗑
|
||||
HYDRALAZINE | INCREASES NITRIC OXIDE AND K CHANNELS TO CAUSE VASODILATION
🗑
|
||||
MINOXIDIL | K CHANNEL OPENER
🗑
|
||||
BUMETANIDE | BLOCKS REABSORPTION OF SODIUM AND WATER IN THE ASCENDING LIMB OF LOOP OF HENLE
🗑
|
||||
CARVEDILOL | ALPHA 1 AND BETA 1 , 2 BLOCKER ; VENTRICULAR FAILURE
🗑
|
||||
PRAVASTATIN | HMG CoA REDUCTASE INHIBITOR
🗑
|
||||
CHOLESTYRAMINE | BILE ACID BINDING RESINS; USED IN HYPERCHOLESTEROLEMIA
🗑
|
||||
COLESTIPOL | BILE ACID BINDING RESINS; USED IN HYPERCHOLESTEROLEMIA
🗑
|
||||
COLESELVAM | BILE ACID BINDING RESINS; USED IN HYPERCHOLESTEROLEMIA
🗑
|
||||
EZETIMIBE | INHIBITS INTESTINAL ABSORPTION OF CHOLESTEROL
🗑
|
||||
GEMFIBROZIL | LpL ACTIVATORS
🗑
|
||||
FENOFIBRATE | LpL ACTIVATORS
🗑
|
||||
BEZAFIBRATE | LpL ACTIVATORS
🗑
|
||||
NIACIN / NICOTINIC ACID | INHIBITS APO B CONTAINING LIPOPROTEINS
🗑
|
||||
DIMENHYDRINATE | ANTI HISTAMINIC (I) ; ANTI MOTION
🗑
|
||||
DIPHENHYDRAMINE | ANTI HISTAMINIC (I) ; ANTI MOTION SICKNESS , ANTI PARKINSONS , LOCAL ANAESTHETIC
🗑
|
||||
DOXYLAMINE | ANTI HISTAMINIC (I) ; SLEEP AID
🗑
|
||||
HYDROXYZINE | ANTI HISTAMINIC (I) ; ANTI EMETIC
🗑
|
||||
PROMETHAZINE | ANTI HISTAMINIC (I); ANTI EMETIC , ANTI PARKINSON , LA
🗑
|
||||
CYCLIZINE | ANTI HISTAMINIC (I); ANTI MOTION
🗑
|
||||
MECLIZINE | ANTI HISTAMINIC (I) ; anti motion
🗑
|
||||
FEXOFENADINE | ANTI HISTAMINIC (II) ; ANTI INFLAMMATORY
🗑
|
||||
CETIRIZINE | ANTI HISTAMINIC (II) ;
🗑
|
||||
LEVOCETIRIZINE | ANTI HISTAMINIC (II) ;
🗑
|
||||
DESLORATIDINE | ANTI HISTAMINIC (II) ; ANTI INFLAMMATORY
🗑
|
||||
LORATADINE | ANTI HISTAMINIC (II) ;
🗑
|
||||
CIMETIDINE | ANTI H2 ; BLOCK SECRETION OF GASTRIC ACID
🗑
|
||||
RANITIDINE | ANTI H2 ; BLOCK SECRETION OF GASTRIC ACID
🗑
|
||||
FAMOTIDINE | ANTI H2 ; BLOCK SECRETION OF GASTRIC ACID
🗑
|
||||
NIZATIDINE | ANTI H2 ; BLOCK SECRETION OF GASTRIC ACID
🗑
|
||||
CROMOLYN SODIUM | HISTAMINE RELEASE INHIBITORS ; ASTHMA , RHINITIS
🗑
|
||||
NEDOCROMOLYN SODIUM | HISTAMINE RELEASE INHIBITORS ; ASTHMA , RHINITIS
🗑
|
||||
KETOTIFEN | ANTI H1 WITH MAST CELL STABILISING ACTION
🗑
|
||||
BUSPIRONE | 5 HT AGONISTS ; ANTI ANXIETY
🗑
|
||||
SUMATRIPTAN | 5HT1B , 5HT1C AGONIST , ANTI MIGRAINE
🗑
|
||||
CISAPRIDE | 5HT4 AGONISTS , GASTROESOPHAGEAL REFLUX
🗑
|
||||
RENZAPRIDE | 5HT4 AGONISTS , GASTROESOPHAGEAL REFLUX
🗑
|
||||
TEGASEROD | 5HT4 PARTIAL AGONIST , IRRITABLE BOWEL SYNDROME
🗑
|
||||
DEXFENFLURAMINE | NON SELECTIVE 5HT RECEPTOR AGONIST , SPPETITE SUPRESSANT
🗑
|
||||
LSD | NON SELECTIVE 5HT AGONIST ; HALLUCINOGEN
🗑
|
||||
KETANSERIN | 5HT2A ANTAG , ANTI HYPERTENSIVE , RAYNAUDS DISEASE
🗑
|
||||
RITANSERIN | 5HT2A ANTAG
🗑
|
||||
ONDANSETRON | 5HT3 ANTAG , POST OP ANTIEMETIC , CHEMOTHERAPY INDUCED ALSO
🗑
|
||||
DOLASETRON | 5HT3 ANTAG , POST OP ANTIEMETIC
🗑
|
||||
GRANISETRON | 5HT3 ANTAG , POST OP ANTIEMETIC
🗑
|
||||
CLOZAPINE | 5HT AND DOPAMINE ANTAG , ANTIPSYCHOTIC
🗑
|
||||
OLANZAPINE | 5HT AND DOPAMINE ANTAG , ANTIPSYCHOTIC
🗑
|
||||
RISPERIDONE | 5HT AND DOPAMINE ANTAG , ANTIPSYCHOTIC
🗑
|
||||
METHYLSERGIDE | 5HT 2A ANTAG ; USED IN MIGRAINE PROPHYLAXIS
🗑
|
||||
CYPROHEPTADINE | 5HT 2A ANTAG , POSTGASTRECTOMY AND CARCINOID
🗑
|
||||
ERGOTAMINE | PARTIAL AGONIST 5HT ,
🗑
|
||||
BROMOCRIPTINE | PARTIAL AGONIST 5HT , PARKINSON
🗑
|
||||
ERGOMETRINE | PARTIAL AGONIST 5HT , PREVENT POST PARTUM HAEMORRHAGE
🗑
|
||||
DINOPROSTONE | PGE2 ; INDUCING ABORTION , LABOUR AND POST PARTUM HAEMORRHAGE PREVENTION
🗑
|
||||
MISOPROSTOL | PGE2 ; ABORTIFACIENT , PEPTIC ULCER
🗑
|
||||
CARBOPROST | PGF2ALPHA , ABORTIFACIENT , LABOUR AND POST PARTUM HAEMORRHAGE PREVENTION
🗑
|
||||
ENPROSTIL | PGE2 , PEPTIC ULCER
🗑
|
||||
EPOPROSTENOL | PGI2 , PREVENT PLATELET AGGREG , DUCTUS ARTERIOSUS , PULMONARY HYPERTENSION
🗑
|
||||
LATANOPROST | PGF2 ALPHA , USED IN GLAUCOMA
🗑
|
||||
ALPROSTADIL | PGE1 , NALE IMPOTENCE
🗑
|
||||
ZAFIRLUKAST | cys LT RECEPTOR ANTAG
🗑
|
||||
MONTELEUKAST | cys LT RECEPTOR ANTAG
🗑
|
||||
IRALUKAST | cys LT RECEPTOR ANTAG
🗑
|
||||
ZILEUTON | LIPOOXYGENASE INHIBITOR ; ANTI ASTHMA AND ANTIINFLAMMATORY
🗑
|
||||
SULFASALAZINE | NONSELECTIVE IRREVERSIBLE OF COX , ULCERATIVE COLITIS , ARTHRITIS
🗑
|
||||
SODIUM SALICYLATE | NONSELECTIVE IRREVERSIBLE OF COX
🗑
|
||||
METHYL SALICYLATE | NONSELECTIVE IRREVERSIBLE OF COX
🗑
|
||||
PHENYLBUTAZONE | NON SELECTIVE REVERSIBLE COX
🗑
|
||||
OXYPHENBUTAZONE | NON SELECTIVE REVERSIBLE COX
🗑
|
||||
IBUPROFEN | NON SELECTIVE REVERSIBLE COX
🗑
|
||||
KETOPROFEN | NON SELECTIVE REVERSIBLE COX
🗑
|
||||
MEFENAMIC ACID | NON SELECTIVE REVERSIBLE COX , DYEMENNORHOEA , OSTEOARTHRITIS
🗑
|
||||
FLUFENAMIC ACID | NON SELECTIVE REVERSIBLE COX
🗑
|
||||
PIROXICAM | NON SELECTIVE REVERSIBLE COX , ACUTE GOUT
🗑
|
||||
KETOROLAC | NON SELECTIVE REVERSIBLE COX , CONJUNCTIVITIS
🗑
|
||||
DICLOFENAC | NON SELECTIVE REVERSIBLE COX
🗑
|
||||
NIMESULIDE | WEAK INHIB OF COX1 AND COX2
🗑
|
||||
ETODOLAC | PREFERENTIAL COX2
🗑
|
||||
ROFECOXIB | SELECTIVE COX2
🗑
|
||||
VAKDECOXIB | SELECTIVE COX2
🗑
|
||||
PARACETAMOL | COX3 OR REVERSIBLE OF COX1
🗑
|
||||
NEFOPAM | NO INHIBITION OF PGs
🗑
|
||||
ASPIRIN | NON SLEECTIVE IRREVERSIBLE OF COX , DUCTUS ARTERIOSUS CLOSURE , PRE ECCLAMPSIA , COLON AND RECTAL CANCER , ALZHEIMERS , FAMILIAL COLONIC POLYPOSIS , SLOWDOWN CATARACT
🗑
|
||||
SALICYLIC ACID | NON SELECTIVE IRREVERSIBLE COX INHIB , KERATOLYTIC
🗑
|
||||
INDOMETHACIN | NON SELECTIVE REVERSIBLE COX INHIB
🗑
|
||||
COLCHICINE | INHIBITS NEUTROPHIL MIGRATION INTO THE JOINTS ; ACUTE GOUT
🗑
|
||||
PREDNISOLONE | SUPRESSES INFLAMMATION ; ACUTE GOUT
🗑
|
||||
ALLOPURINOL | INHIBITS XANTHINE OXIDASE , SO URIC ACID ; CHRONIC GOUT
🗑
|
||||
PROBENECID | PROMOTES EXCRETION OF URIC ACID ; CHRONIC GOUT
🗑
|
||||
SULFINPYRAZONE | PREVENTS REABSORPTION OF URIC ACID
🗑
|
||||
INFLIXIMAB | INHIBITS T CELL AND MACROPHAGE
🗑
|
||||
LEFLUNOMIDE | INHIBITS T CELL AND ANTIBODY PRODUCTION ; IMMUNOMODULATOR
🗑
|
||||
METHOTREXATE | FOLIC ACID ANTAG ; IMMUNOMODULATOR
🗑
|
||||
CYCLOSPORINE | INHIBITS IL1 AND IL2 RECEPTORS ; INHIBITS T CELL INTERACTION AND RESPONSIVENESS
🗑
|
||||
AZATHIOPRINE | PRO DRUG OF 6 MERCAPTOPURINE MAKES A NON FUNCTIONAL NA WHICH IS INCORPORATED INTO DNA AND IS NON FUNCTIONAL ; INHIBITS T CELLS ; USED IN GRAFT TRANSPLANT
🗑
|
||||
AURANOFIN | ALTERS MORPHOLOGY OF MACROPHAES AND PREVENTS JOINT DESTRUCTION
🗑
|
||||
HYDROXYCHLOROQUINE | SUPRESS T CELL FUNCTION ; RA
🗑
|
||||
SULFASALAZINE | ORAL , NON ABSORBABLE .IT IS METABOLISED TO SULFAPYRIDINE AND 5 ASA ; SULFAPYRIDINE MIGRATES TO JOINTS AND USED , WHILE 5 ASA IS USED IN RA
🗑
|
||||
CYCLOPHOSPHAMIDE | CROSS LINKS DNA TO PREVENT CELL REPLICATION ; CANCER AND RA AS IMMUNOSUPRESSANT
🗑
|
||||
SUCRALFATE | POLYMERISES BY CROSS LINKING OF MOLECULES TO FORM A GEL OVER THE ULCER
🗑
|
||||
COLLOIDAL BISMUTH SUBCITRATE | IT CONVERTS INTO BISMUTH OXYCHLORIDE AND THEN CHELATES WITH GLYCOPROTEINS TO FORM A GEL OVER THE ULCER
🗑
|
||||
PANTOPRAZOLE | BLOCKS H+/K+/ATPase AND PREVENTS FORMATION OF ACID
🗑
|
||||
OMEPRAZOLE | BLOCKS H+/K+/ATPase AND PREVENTS FORMATION OF ACID
🗑
|
||||
ESOMEPRAZOLE | BLOCKS H+/K+/ATPase AND PREVENTS FORMATION OF ACID
🗑
|
||||
SODIUM ALGINATE | FORMS A GEL WITH THE ACID
🗑
|
||||
SODIUM BICARBONATE | SYSTEMIC ANTACID , barb poisoning
🗑
|
||||
ALUMINIUM HYDROXIDE | NON SYSTEMIC BUFFER ANTACID
🗑
|
||||
MAGNESIUM TRISILICATE | NON SYSTEMIC BUFFER ANTACID
🗑
|
||||
CALCIUM CARBONATE | NON SYSTEMIC NON BUFFER ANTACID
🗑
|
||||
MAGNESIUM HYDROXIDE | NON SYSTEMIC NON BUFFER ANTACID
🗑
|
||||
CARBENOXOLONE SODIUM | INCREASES PRODUCTION OF MUCUS
🗑
|
||||
CLARITHROMYCIN | BLOCKS 50S RIBOSOMES ; ANTI HELICOBACTER
🗑
|
||||
AMOXICILLIN | PENICILLIN GRP ; ANTI HELICOBACTER
🗑
|
||||
METRONIDAZOLE | ANAEROBIC ; ANTI HELICOBACTER
🗑
|
||||
CINNARIZINE | ANTI HISTAMINIC , CALCIUM BLOCKER ; MOTION SICKNESS
🗑
|
||||
PROCHLORPERAZINE | 5HT3 ANTAG AND D2 BLOCKING ANTAGS ; CHEMO INDUCED VOMITING
🗑
|
||||
METOCLOPRAMIDE | DOPAMINE BLOCKER ; CHEMO INDUCED VOMITING
🗑
|
||||
DOMPERIDONE | D2 ANTAG ; CHEMO INDUCED VOMITING
🗑
|
||||
DROPERIDOL | ANTI PSYCHOTIC
🗑
|
||||
LOXIGLUMIDE | CCK1 ANTAG ; INCREASES GI MOTILITY
🗑
|
||||
LOPERAMIDE | CODEINE ANALOGUE ; ANTI DIARRHOEALS
🗑
|
||||
LACTULOSE | INCREASE THE OSMOLARITY OF THE LUMINAL CONTENTS THEREBY INCREASING THE STIMULATION OG THE GUT WALLS FOR PERISTALSIS
🗑
|
||||
LIQUID PARAFFIN | Luminally active
🗑
|
||||
Docusate | DECREASES SURFACE TENSION OF FLUIDSM
🗑
|
||||
MAGNESIUM SULFATE | INCREASE OSMOLARITY AND HENCE THE BULK BY DRAWING WATER , PREVENTS CONVULSIONS AND REDUCES BP IN PRE ECCLAMPSIA AND ECCLAMPSIA PATIENTS
🗑
|
||||
POLYETHYLENE GLYCOL | HIGHLY OSMOTIC , SO IT RETAINS WATER AND INCREASES THE BULK
🗑
|
||||
ALOE | IRRITATE THE WALL AND STIMULATE PERISTALSIS
🗑
|
||||
CASTOR OIL | IRRITATE THE WALL ANC STIMULATES PERISTALSIS
🗑
|
||||
RACECADOTRIL | ENKEPHALINASE INHIBITOR WHICH INCREASES ENKEPHALINS AND IRRITATES THE WALL AND STIMULATES PERISTALSIS
🗑
|
||||
OCTREOTIDE | REDUCES MOTILITY OF GI
🗑
|
||||
CHENODEOXYCHOLIC ACID | REDUCES CH , HMGCOA REDUCTASE INHIB , INCREASES LITHOLYTIC
🗑
|
||||
URSODIOL | INHIBITS ABSORPTION OF CHOLESTEROL , REDUCES CH , LOWERS SATURATION INDEX OF BILE , SO THAT IT ISN'T LITHOGENIC
🗑
|
||||
HALOTHANE | INHALATIONAL ANAESTHETIC
🗑
|
||||
PROPOFOL | INTRAVENOUS ANAESTHETIC
🗑
|
||||
ETOMIDATE | INTRAVENOUS ANAESTHETIC
🗑
|
||||
KETAMINE | DISSOCIATIVE ANAESTHETIC , calmness and psychic indifference without loss of consciousness and analgesia , non competitive blocker of nmda
🗑
|
||||
METHOXYFLURANE | INHALATIONAL ANAESTHETIC
🗑
|
||||
ISOFLURANE | INTRAVENOUS ANAESTHETIC
🗑
|
||||
CHLORDIAZEPOXIDE | BENZODIAZEPINE , ANXIOLYTICS
🗑
|
||||
ZOPICLONE | BZ1 RECEPTORS AND HAVE HYPNOTIC
🗑
|
||||
ZOLPIDEM | BZ1 RECEPTOR
🗑
|
||||
ZALEPLON | BZ1 receptor
🗑
|
||||
FLUMAZENIL | BZD ANTAG
🗑
|
||||
IPSASPIRONE | 5HT1 agonist
🗑
|
||||
GESPIRONE | 5HT1 AGONIST
🗑
|
||||
THIOPENTAL | ACTS ON CHANNEL MODULATORY SITE OF GABA , INCREASES DURATION OF CHLORIDE
🗑
|
||||
METHOHECITAL | BARB , ultra short acting
🗑
|
||||
PHENOBARBITAL | BARB , long acting
🗑
|
||||
PENTOBARB | Short acting
🗑
|
||||
DESIPRAMINE | BLOCKS EOINEPHRINE
🗑
|
||||
NORTRYPTILLINE | CLOCKS EPINEPHRINE
🗑
|
||||
PROTRIPTYLINE | BLOCKS EPINEPHRINE
🗑
|
||||
SERTRALINE | INCREASE SEROTONIN IN SYNAPTIC CLEFT BY PREVENTING NEURONAL UPTAKE
🗑
|
||||
FLUOXETINE | INCREASE SEROTONIN IN SYNAPTIC CLEFT BY PREVENTING NEURONAL UPTAKE
🗑
|
||||
CITALOPRAM | INCREASE SEROTONIN IN SYNAPTIC CLEFT BY PREVENTING NEURONAL UPTAKE
🗑
|
||||
FLUVOXAMINE | INCREASE SEROTONIN IN SYNAPTIC CLEFT BY PREVENTING NEURONAL UPTAKE
🗑
|
||||
PAROXETINE | INCREASE SEROTONIN IN SYNAPTIC CLEFT BY PREVENTING NEURONAL UPTAKE
🗑
|
||||
TRAZODONE | INHIBITS UPTAKE OF 5HT
🗑
|
||||
MIANSERIN | BLOCKS ALPHA 2
🗑
|
||||
MIRTAZAPINE | 5 HT1
🗑
|
||||
SELEGILINE | INHIBIT MAO B
🗑
|
||||
LITHIUM | INHIBITS IP2 TO IP1 AND IP1 TO IP
🗑
|
||||
ETHANOL | CNS DEP , DEC OF MYOCARDIUM , CUTANEOUS VASODILATION , DIURESIS , RESP DEPRESSION , IRRITABILITY
🗑
|
||||
MORPHINE | Increases pain threshold , euphoria , anaesthetic , cough suppressant , diarrhoea ,
🗑
|
||||
NALOXONE | ANTAG TO MORPHINE
🗑
|
||||
PENTAZOCINE | WEAK ANTAG OF MU , AG OF KAPPA A ND WEAK AG OF DELTA
🗑
|
||||
BUPRENORPHINE | PARTIAL AG OF MU , ANTAG OF KAPPA ,
🗑
|
||||
NALTREXONE | ANTAG OF MORPHEINE
🗑
|
||||
CARBAMAZEPINE | BLOCKS Na CHANNELS , TRIGEMINAL ANALGESIA
🗑
|
||||
ETHISUXIMIDE | BLOCKS Ca channels
🗑
|
||||
VALPROIC ACID | BLOCKS NA , GLUTAMATE , INHIBITS GABA TRANSAMINASE ,
🗑
|
||||
Vigabatrin | IRREVERSIBLE INHIBITOR OF GABA TRANSAMINASE
🗑
|
||||
TIAGABINE | INHIBIT GABA UPTAKE
🗑
|
||||
TOPIRAMATE | BLOCKS NA CHANNELS , INCREASES GABA , INHIBITS GLUTAMATE
🗑
|
||||
LAMOTRIGINE | DIRECTLY BLOCKS Na channel
🗑
|
||||
FELBAMATE | BLOCKS NMDA
🗑
|
||||
TOLCAPONE | COMT INHIB
🗑
|
||||
ENTACAPONE | Comt INHIB
🗑
|
||||
AMANTADINE | PREVENTS DOPAMINE UPTAKE AND FACILITATES PRESYNAPTIC RELEASE OF DA , BLOCKS NMDA , ANTI MUSCARINIC
🗑
|
||||
SALBUTAMOL | BETA BLOCKER. , TOCOLYTIC
🗑
|
||||
TERBUTALINE | BETA BLOCKER , TOCOLYTIC
🗑
|
||||
NIFEDIPINE | PERIPHERAL VASODILATOR , TOCOLYTIC
🗑
|
||||
METYRAPONE | 11 BETA HYDROXYLASE ENZYME INHIBITOR
🗑
|
||||
AMINOGLUTETHAMIDE | BLOCKS CONVERSION OF CHOLESTEROL TO PREGNENOLONE
🗑
|
||||
MITOTANE |
🗑
|
||||
CLOMIPHENE | SSRM , INCREASES FSH AND LH
🗑
|
||||
TAMOXIFEN | ANTAG OF ESTROGEN IN BREAST AND AG OF ESTROGEN IN UTERUS , BONE , PITUITARY , LIVER
🗑
|
||||
DOLOXIFEN | ANTAG OF ESTROGEN IN BREAST , AG IN BONE , LIVER , PITUITARY
🗑
|
||||
TOREMIFEN | ANTAG IN BREAST , AG IN BONE M LIVER , PITUITARY , UTERUS
🗑
|
||||
FULVESTRANT | ANTAG IN BREAST , AG IN BONE , LIVER , PITUITARY AND UTERUS
🗑
|
||||
RALOXIFENE | ANTIESTROGEN IN BREAST , ENDOMETRIUM , ESTROGEN IN BONE , COAGULATION OF BLOOD , LIPID META
🗑
|
||||
CENTCHROMAN | SERM
🗑
|
||||
MIFEPRISTONE | BLOCKS PROGESTERONE
🗑
|
||||
GOSSYPOL | REDUCES SPERM COUNT AND MOTILITY
🗑
|
||||
ANASTROZOLE | INHIBIT AROMATASE AND SO ESTROGEN
🗑
|
||||
LETROZOLE | INHIBIT AROMATASE AND SO ESTROGEN
🗑
|
||||
FADROZOLE | INHIBIT AROMATASE AND SO ESTROGEN
🗑
|
||||
VOROZOLE | INHIBIT AROMATASE AND SO ESTROGEN
🗑
|
||||
LEVOTHYROXINE | T4
🗑
|
||||
CARBIMAZOLE | INHIBITS THYROID PEROXIDASE , INCORPORATION OF IODINE INTO THE TYROSINE , AND INHIB OF COUPLING OF IODITYROSYL RESIDUES
🗑
|
||||
METHIMAZOLE | INHIBITS THYROID PEROXIDASE , INCORPORATION OF IODINE INTO THE TYROSINE , AND INHIB OF COUPLING OF IODITYROSYL RESIDUES
🗑
|
||||
LUGOLS IODINE | INCREASEDIODINE INHIBITS ITS OWN TRANSPORT AS WELL AS THE RELEASE OF THE HORMONE
🗑
|
||||
PERCHLORATE | COMPETITIVE INHIBITOR OF THYROIDAL IODINE TRANSPORT VIA THE Na/I TRANSPORTER
🗑
|
||||
THIOCYANATE | COMPETITIVE INHIBITOR OF THYROIDAL IODINE TRANSPORT VIA THE Na/I TRANSPORTER
🗑
|
||||
INSULIN LISPRO | ULTRA SHORT ACTING
🗑
|
||||
INSULIN ASPARTAME | ULTRA SHORT ACTING
🗑
|
||||
INSULIN ZINC SUSPENSION /SEMILENTE | SHORT ACTING
🗑
|
||||
ISOPHANE INSULIN /LENTE | INTERMEDIATE ACTING
🗑
|
||||
INSULIN GLARGINE | LONG ACTING
🗑
|
||||
UKTRALENTE | LONG ACTING
🗑
|
||||
TOLBUTAMIDE | BLOCKS K CHANNELS AND INCREASES CALCIUM AND HENCE STIMULATES B CELLS TO SECRETE INSULIN ulfonylurea
🗑
|
||||
CHLORPROPAMIDE | BLOCKS K CHANNELS AND INCREASES CALCIUM AND HENCE STIMULATES B CELLS TO SECRETE INSULIN sulfonylurea
🗑
|
||||
REPAGLINIDE | BLOCKS K CHANNELS AND INCREASES CALCIUM AND HENCE STIMULATES B CELLS TO SECRETE INSULIN meglitinide analogues
🗑
|
||||
NATEGLINIDE | BLOCKS K CHANNELS AND INCREASES CALCIUM AND HENCE STIMULATES B CELLS TO SECRETE INSULIN meglitinide
🗑
|
||||
METFORMIN | iNCREASES UPTAKE AND UTIKISATION OF GLUCOSE AND PREVENTS GLUCONEOGENESIS AND GLYCIGEN AND INCREASES BINDUNG OF INSUKIN TO ITS RECEPTOR , SLOWS GLUCOSE ABSORPTION FROM THE STOMACH, biguanids
🗑
|
||||
PHENFORMIN | iNCREASES UPTAKE AND UTIKISATION OF GLUCOSE AND PREVENTS GLUCONEOGENESIS AND GLYCIGEN AND INCREASES BINDUNG OF INSUKIN TO ITS RECEPTOR , SLOWS GLUCOSE ABSORPTION FROM THE STOMACH , biguanides
🗑
|
||||
ACARBOSE | Inhibits alpha gkycosidase and thus absorption of glucose
🗑
|
||||
MIGLITO | Inhibits alpha gkycosidase and thus absorption of glucose
🗑
|
||||
ROSIGLITAZONE | AGONIST TO PPAR GAMMA WHICH BINDS WITH RETINOID X RECEPTOR WHICH INCREASES LIPOGENESIS AND PROMOTES UPTAKE OF FATTY ACIDSAND GLUCOSE
🗑
|
||||
PIOGLITAZONE | AGONIST TO PPAR GAMMA WHICH BINDS WITH RETINOID X RECEPTOR WHICH INCREASES LIPOGENESIS AND PROMOTES UPTAKE OF FATTY ACIDSAND GLUCOSE
🗑
|
||||
CODEINE | CENTRALLY ACTING ANTITUSSIVE
🗑
|
||||
DEXTROMETHORPHAN | CENTRALLY ACTING ANTITUSSIVE
🗑
|
||||
BENZONATATE | INHIBITS PERIPHERAL RECEPTORS AND CENTRAL COUGH CENTRE AFFERENTS
🗑
|
||||
PRENOXDIAZINE | SUPRESSES PERIPHERAL RECEPTORS
🗑
|
||||
AMMONIUM CHLORIDE | STIMULATES BRONCHIAL CELLZ TI SECRETE MUCUS AND CIKIA TO CLEAR IT mucokinetic
🗑
|
||||
SODIUM CITRATE | STIMULATES BRONCHIAL CELLZ TI SECRETE MUCUS AND CIKIA TO CLEAR IT mucokinetic
🗑
|
||||
ACETYL CYSTEINE | MUCOLYTIC DECREASES VISCOSITY OF MUCUS BY SPLITTING DISULFIDE BONDS OF MUCOPROTEIN
🗑
|
||||
BROMHEXINE | DEPOLYMERISES MUCOPOLYSACCHARIDES OF MUCUS
🗑
|
||||
DORNASE ALFA | DNAase SPLITS DNA
🗑
|
||||
SULFACYTINE | ORAL , SHORT ACTING SULFONAMIDE
🗑
|
||||
SULFADIAZINE | ORAL , SHORT ACTING
🗑
|
||||
SULFISOXOZOLE | ORAL , SHORT ACTING
🗑
|
||||
SULFAMETHAZOLE | ORAL SHORT ACTING SULFONAMIDE
🗑
|
||||
SULFAMETHAXOZOLE | ORAL INTERMEDIATE ACTING SULFONAMIDE
🗑
|
||||
SULFADOXINE | ORAL LONG ACTING SULFONAMIDE
🗑
|
||||
OLSALAZINE | ORAL NON ABSORBABLE SULFONAMIDE
🗑
|
||||
SILVER SULFADIAZINE | TOPICAL SULFONAMIDE
🗑
|
||||
SULFACETAMIDE | TOPICAL SULFONAMIDE
🗑
|
||||
NORFLOXACIN | FIRST GENERATION FLUOROQUINOLONES
🗑
|
||||
CIPROFLOXACIN | FIRST GENERATION FLUOROQUINOLONES
🗑
|
||||
OFLOXACILIN | FIRST GENERATION FLUOROQUINOLONES
🗑
|
||||
PEFLOXACIN | FIRST GENERATION FLUOROQUINOLONES
🗑
|
||||
LOMEFLOXACIN | FIRST GENERATION FLUOROQUINOLONES
🗑
|
||||
LEVOFLOXACIN | SECOND GENERATION FLUOROQUINOLONES
🗑
|
||||
GATIFLOXACIN | THIRD GENERATION FLUOROQUINOLONES
🗑
|
||||
SPARFLOXACIN | THIRD GENERATION FLUOROQUINOLONES
🗑
|
||||
MOXIFLOXACIN | FOURTH GENERATION FLUOROQUINOLONES
🗑
|
||||
ALATROFLOXACIN | FOURTH GENERATION FLUOROQUINOLONES
🗑
|
||||
TROVAFLOXACIN | FOURTH GENERATION FLUOROQUINOLONES
🗑
|
||||
PHENAZOPYRIDINE | URINARY ANALGESIC ;
🗑
|
||||
NITROFURANTOIN | INHIBITS ACETYL COA WHICH BLOCKS CARB META AND SO THE BACTERIA ; URINARY ANTISEPTIC
🗑
|
||||
NALIDIXIC ACID | NON FLUORINATED QUINOLONES ; URINARY ANTISEPTICS
🗑
|
||||
PENICILLIN V | ORAL NATURAL PENICILLIN
🗑
|
||||
PENICILLIN G | IM OR IV NATURAL PENICILLIN
🗑
|
||||
PROCAINE PENICILLIN | IM DEPOT ; BETA LACTAMASE SENSITIVE
🗑
|
||||
BENZATHINE PENCILLIN | IM DEPOT ; BETA LACTAMASE PENICILLIN
🗑
|
||||
CLOXACILLIN | ORAL LACTAMASE RESISTANT PENICILLIN
🗑
|
||||
DICLOXACILLLIN | ORAL LACTAMASE RESISTANT PENICILLIN
🗑
|
||||
METHICILLIN | IM OR IV LACTAMASE RESISTANT PENICILLIN
🗑
|
||||
CLAVULANIC ACID | BETA LACTAMASE INHIBITOR ; BIND IRREVERSIBLY TO THE CATALYTIC SITE OF LACTAMASE
🗑
|
||||
SULBACTAM | BETA LACTAMASE INHIBITOR
🗑
|
||||
TAZOBACTAM | BETA LACTAMASE INHIBITOR
🗑
|
||||
CEFAZOLIN | FIRST GENERATION CEPALOSPORIN
🗑
|
||||
CEFALOTHIN | FIRST GENERATION CEPHALOSPORIN
🗑
|
||||
CEFADROXIL | FIRST GENERATION CEPHALOSPORIN
🗑
|
||||
CEFARADINE | FIRST GENERATION CEPHALOSPORIN
🗑
|
||||
CEFUROXIME | SECOND GENERATION CEPHALOSPORIN ORAL
🗑
|
||||
CEFOXITIN | SECOND GENERATION CEPHALOSPORIN PARENTERAL
🗑
|
||||
CEFACLOR | SECOND GENERATION CEPHALOSPORIN ORAL
🗑
|
||||
CEFOTETAN | SECOND GENERATION CEPHALOSPORIN PARENTERAL
🗑
|
||||
CEFIXIME | THIRD GENERATION CEPHALOSPORIN ORAL
🗑
|
||||
CEFTIZOXIME | THIRD GENERATION CEPHALOSPORIN PARENTERAL
🗑
|
||||
CEFTRIAXONE | THIRD GENERATION CEPHALOSPORIN PARENTERAL
🗑
|
||||
CEFDINIR | THIRD GENERATION CEPHALOSPORIN ORAL
🗑
|
||||
CEFPODOXIME | THIRD GENERATION CEPHALOSPORIN ORAL
🗑
|
||||
CEFPEROME | FOURTH GENERATION CEPHALOSPORIN PARENTERAL
🗑
|
||||
CEFIPIME | FOURTH GENERATION CEPHALOSPORIN PARENTERAL
🗑
|
||||
AZTREONAM | NEWER BETA LACTAM ANTIBIOTICS
🗑
|
||||
CARBAPENEM | NEWER BETA LACTAM
🗑
|
||||
VANCOMYCIN | INHIBITS GRAM POSITIVE CELL WALL SYNTHESIS BY COMPLEXING D ALANYL D ALANINE PORTION OF TERMINAL END OF PEPTIDOGLYCAN
🗑
|
||||
TEICOPLANIN | INHIBITS GRAM POSITIVE CELL WALL SYNTHESIS BY COMPLEXING WITH D ALANYL D ALANINE PORTION OF THE TERMINAL END OF THE PEPTIDOGLYCAN
🗑
|
||||
BACITRACIN | BLOCKS THE FUNCTION OF LIPID CARRIER MOLECULES WHICH TRANSFERS CELL WALL SUBUNITS ACROSS CELL MEMBRANE
🗑
|
||||
FOSFOMYCIN | INHIBITS BACTERIAL CELL WALL SYNTHESIS BY INACTIVATING PYRUVYL TRANSFERASE WHICH IS CRUCIAL FOR THE FORMATION OF UDP N ACETYL MURAMIC ACID WHICH IS FOUND IN THE CELL WALL
🗑
|
||||
STREPTOMYCIN | AMINOGLYCOSIDE
🗑
|
||||
GENTAMYCIN | AMINOGLYCOSIDE
🗑
|
||||
KANAMYCIN | AMINOGLYCOSIDE
🗑
|
||||
AMIKACIN | AMINOGLYCOSIDE
🗑
|
||||
NEOMYCIN | AMINOGLYCOSIDE , TOPICAL
🗑
|
||||
SOFRAMYCIN | AMINOGLYCOSIDE TOPICAL
🗑
|
||||
PAROMOMYCIN | AMINOGLYCOSIDE , TOPICAL
🗑
|
||||
ERYTHROMYCIN | MACROLIDE
🗑
|
||||
ROXITHROMYCIN | MACROLIDE
🗑
|
||||
CLARITHROMYCIN | MACROLIDE
🗑
|
||||
AZITHROMYCIN | MACROLIDE
🗑
|
||||
SPIRAMYCIN | MACROLIDE
🗑
|
||||
CLINDAMYCIN | LINCOSAMIDE
🗑
|
||||
TELITHROMYCIN | KETOLIDE
🗑
|
||||
LINEZOLID | OXAZOLIDINONE
🗑
|
||||
PRISTINNAMYCIN | COMBI OF STREPTOGRAMIN B AND STREPTOGRAMIN A IN A 30 : 70 RATIO ; BINDS TO 50S ( STREPTOGRAMINS)
🗑
|
||||
POLYMYXIN B | DISRUPTS THE BACTERIAL CELL MEMBRANE OSMOTIC INTEGRITY BY DISPLACING CALCIUM AND MAGNESIUM FROM MEMBRANE LIPID PHOSPHATES
🗑
|
||||
MUPIROCIN | INHIBITS BACTERIAL RNA AND PROTEIN SYNTHESIS BY BINDING TO ISOLEUCYL T RNA SYNTHETASE
🗑
|
||||
FUSIDIC ACID | INHIBITS PROTEIN ELONGATION
🗑
|
||||
TETRACYCLINE |
🗑
|
||||
CHLORAMPHENICOL |
🗑
|
||||
DOXYCYCLINE | TETRACYCLINE
🗑
|
||||
DEMECLOCYCLINE | TETRACYCLINE
🗑
|
||||
MINOCYCLINE | TETRACYCLINE
🗑
|
||||
ISONIAZID | INHIBITS SYNTHESIS OF MYCOLIC ACID WHICH IS AN ESSENTIAL COMPONENT OF MYCOBACTERIAL CELL WALL
🗑
|
||||
RIFAMPICIN | BINDS STRONGLY TO THE BETA SUBUNIT OF BACTERIAL DNA DEPENDENT RNA POLYMERASE , SO INHIBITS RNA SYNTHESIS
🗑
|
||||
ETHAMBUTOL | INHIBITS ARABINOSYL TRANSFERASE ENZYME TO PREVENT POLYMERISATION OF ARABINOGLYCANS IN MYCOBACTERIAL CELL WALL
🗑
|
||||
PYRAZINAMIDE | IT ENTERS THE MYCOBACTERIUM AND GETS CONVERTED TO PYRAZINOIC ACID BY BACTERIAL PYRAZINAMIDASE WHICH INHIBITS MYCOBACTERIAL FATTY ACID SYNTHASE I AND DISRUPTS MYCOLIC ACID FORMATION
🗑
|
||||
DAPSONE | INHIBITION OF BACTERIAL FOLIC ACID SYNTHESIS
🗑
|
||||
CLOFAZIMINE | BINDS TO THE MYCOBACTERIAL DNA , INTERFERES WITH ITS TEMPLATE FUNCTION AND INHIBITS MYCOBACTERIAL GROWTH
🗑
|
||||
ACLOMETASONE | TOPICAL GLUCOCORTICOID
🗑
|
||||
AMCINONIDE | TOPICAL GLUCOCORTICOID
🗑
|
||||
BELCOMETHASONE | TOPICAL/INHALATIONAL GLUCOCORTICOID
🗑
|
||||
BUDESOINDE | INHALATIONAL GLUCOCORTICOID
🗑
|
||||
FLUCINOLONE | TOPICAL GLUCOCORTICOID
🗑
|
||||
FLUTICASONE | TOPICAL GLUCOCORTICOID
🗑
|
||||
MEDRYSONE | OPTHALMIC GLUCOCORTICOID
🗑
|
||||
LEVOTHYROXINE SODIUM | INCREASES T4 TO T3 AND REDUCES TSH STIMULATION BY NEGATIVE FEEDBACK AND THUS CAN BE USED IN NON ENDEMIC GOITRE ; ALSO USED IN REFRACTORY ANAEMIAS , NON HEALING WOUNDS , CHRONIC CONSTIPATION , MENSTRUAL DISORDERS AND INFERTILITY
🗑
|
||||
LIOTHYRONINE | NOT USED AS MUCH ; MYXOEDEMA COMA , SHORT TERM SUPRESSION OF TSH IN THYROIDECTOMY ,
🗑
|
||||
PROPYLTHIOURACIL | INHIBIT PEROXIDASE , COUPLING , INCORPORATION OF IODINE INTO TYROSYL RESIDUES , AND PERIPHEARL CONVERSION OG T4 TO T3
🗑
|
||||
CARNBIMAZOLE | INHIBIT PEROXIDASE , COUPLING , INCORPORATION OF IODINE INTO TYROSYL RESIDUES , AND PERIPHEARL CONVERSION OG T4 TO T3
🗑
|
||||
METHCARBIMAZOLE | INHIBIT PEROXIDASE , COUPLING , INCORPORATION OF IODINE INTO TYROSYL RESIDUES , AND PERIPHEARL CONVERSION OG T4 TO T3
🗑
|
||||
RADIOACTIVE IODINE | EVALUATING THYROID FUNCTIONS , NON SURGICAL THYROID ABLATION , BETA PARTICLES DESTROY PARENCHYMA
🗑
|
||||
LUOGOLS IODINE | LIMITS ITS OWN TRANSPORT , THYROID HORMONE RELEASE , ; PREPARE PATIENT FOR THYROIDECTOMY , BY MAKING IT LESS VASCULAR AND MORE COMPACT ; TREAT SEVERE THYROTOXICOSIS
🗑
|
||||
PERCHLORATE ION | COMPETITIVE INHIBITOR OF THYROIDAL IODIDE TRANSPORT VIA NA , I TRANSPORTER . RARELY USED CUZ IT CAUSES FATAL APLASTIC ANAEMIA AND GASTRIC ULCERS
🗑
|
||||
THIOCYANATE | COMPETITIVE WITH THE IODIDE TRANSPORTER
🗑
|
||||
ORAL IPODATE | HYPERTHYROID , INHIBIT 5 DEIODINASE AND PREVENT CONVERSION OF T4 TO T3
🗑
|
||||
CASPOFUNGIN | INHIBITS CELL WALL SYNTHESIS
🗑
|
||||
AMPHOTERICIN B | MACROLIDE , BINDS TO ERGOSTEROL , HENCE FORMING PORES CAUSE LEAKING OF IONS AND FURTHER LYSIS
🗑
|
||||
NYSTATIN | BINDS TO ERGOSTEROL AND HENCE FORMS PORES CAUSING LEAKING OF IONS AND FURTHER LYSIS
🗑
|
||||
TERBINAFINE | INHIBITS LANOSTEROL TO ERGOSTEROL BY SQUALENE EPOXIDASE , RESULTING IN ACC OF SQUALENE CAUSING LYSIS
🗑
|
||||
NAFTIFINE | INHIBITS LANOSTEROL TO ERGOSTEROL CAUSING LYSIS
🗑
|
||||
BUTENAFINE | INHIBITS LANOSTEROL TO ERGOSTEROL CAUSING LYSIS
🗑
|
||||
MICONAZOLE | BINDS TO FUNGAL CYTOCHROME P 450 WHICH PREVENTS THE CONVERSION OF LANOSTEROL TO ERGOSTEROL BY 14 ALPHA DEMETHYLASE
🗑
|
||||
KETOCONAZOLE | BINDS TO FUNGAL CYTOCHROME P 450 WHICH PREVENTS THE CONVERSION OF LANOSTEROL TO ERGOSTEROL BY 14 ALPHA DEMETHYLASE
🗑
|
||||
FLUCONAZOLE | BINDS TO FUNGAL CYTOCHROME P 450 WHICH PREVENTS THE CONVERSION OF LANOSTEROL TO ERGOSTEROL BY 14 ALPHA DEMETHYLASE
🗑
|
||||
ITRACONAZOLE | BINDS TO FUNGAL CYTOCHROME P 450 WHICH PREVENTS THE CONVERSION OF LANOSTEROL TO ERGOSTEROL BY 14 ALPHA DEMETHYLASE
🗑
|
||||
VORICONAZOLE | BINDS TO FUNGAL CYTOCHROME P 450 WHICH PREVENTS THE CONVERSION OF LANOSTEROL TO ERGOSTEROL BY 14 ALPHA DEMETHYLASE
🗑
|
||||
GRISEOFULVIN | INTERACTS WITH POLYMERISED MICROTUBULES CAUSING DISRUPTION
🗑
|
||||
TERBINAFINE |
🗑
|
Review the information in the table. When you are ready to quiz yourself you can hide individual columns or the entire table. Then you can click on the empty cells to reveal the answer. Try to recall what will be displayed before clicking the empty cell.
To hide a column, click on the column name.
To hide the entire table, click on the "Hide All" button.
You may also shuffle the rows of the table by clicking on the "Shuffle" button.
Or sort by any of the columns using the down arrow next to any column heading.
If you know all the data on any row, you can temporarily remove it by tapping the trash can to the right of the row.
To hide a column, click on the column name.
To hide the entire table, click on the "Hide All" button.
You may also shuffle the rows of the table by clicking on the "Shuffle" button.
Or sort by any of the columns using the down arrow next to any column heading.
If you know all the data on any row, you can temporarily remove it by tapping the trash can to the right of the row.
Embed Code - If you would like this activity on your web page, copy the script below and paste it into your web page.
Normal Size Small Size show me how
Normal Size Small Size show me how
Created by:
manjari
Popular Pharmacology sets