Tell me MOA,clinical uses,adverse effects and contraindications of these drugs
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| MOA | Irreversibly acetylates and inhibits platelet COX-1 enzyme → blocks thromboxane A2 (TXA2) synthesis → prevents platelet aggregation. At low doses (75–325 mg), antiplatelet effect predominates. |
| Clinical Uses | Antiplatelet: ACS, MI prevention, ischemic stroke, post-CABG, PCI. Also analgesic/antipyretic/anti-inflammatory at higher doses. |
| Adverse Effects | GI ulceration/bleeding, GI upset, tinnitus (high doses), bleeding risk, hypersensitivity (aspirin-exacerbated respiratory disease), Reye's syndrome (children) |
| Contraindications | Active GI ulcer/bleeding, hemophilia, children with viral illness (Reye's), aspirin hypersensitivity/asthma, last trimester of pregnancy |
| MOA | Betamethasone (potent corticosteroid): binds glucocorticoid receptors → suppresses phospholipase A2 → reduces arachidonic acid → anti-inflammatory. Neomycin (aminoglycoside): binds 30S ribosomal subunit → mistranslation of mRNA → bactericidal |
| Clinical Uses | Infected inflammatory skin conditions: infected eczema, infected dermatitis, otitis externa, secondarily infected psoriasis |
| Adverse Effects | Skin atrophy, striae, telangiectasia, hypertrichosis, contact dermatitis to neomycin, HPA axis suppression (if large area/prolonged), local neomycin sensitization |
| Contraindications | Untreated fungal/viral skin infections (herpes, varicella), rosacea, perioral dermatitis, acne, use on face (prolonged), hypersensitivity to neomycin |
| MOA | Dual mechanism: (1) Weak μ-opioid receptor agonist (partial); (2) Inhibits reuptake of serotonin and norepinephrine in descending pain pathways → central analgesia |
| Clinical Uses | Moderate-to-severe pain (post-operative, cancer pain, musculoskeletal, neuropathic pain), chronic pain management |
| Adverse Effects | Nausea, vomiting, dizziness, constipation, somnolence, seizures (dose-related), serotonin syndrome (with SSRIs/MAOIs), dependence/withdrawal, respiratory depression (less than morphine) |
| Contraindications | Concurrent MAOI use, seizure disorders (↓ threshold), acute intoxication with alcohol/opioids/psychotropics, severe hepatic/renal impairment, pregnancy, under 12 years |
| MOA | Competitively inhibits HMG-CoA reductase (rate-limiting enzyme in cholesterol biosynthesis in the liver) → ↓ hepatic cholesterol → upregulation of LDL receptors → ↑ LDL clearance from blood |
| Clinical Uses | Hypercholesterolemia, mixed dyslipidemia, cardiovascular risk reduction (primary & secondary prevention), hypertriglyceridemia; also used in ACS as high-intensity statin |
| Adverse Effects | Myalgia, myopathy, rhabdomyolysis (rare but serious), raised LFTs/hepatotoxicity, headache, GI disturbances, new-onset diabetes mellitus |
| Contraindications | Active liver disease, unexplained persistent ↑ LFTs, pregnancy & breastfeeding, concurrent use with certain antivirals (protease inhibitors), severe renal impairment |
| MOA | Selective PDE-4 inhibitor (phosphodiesterase 4) → ↑ intracellular cAMP → smooth muscle relaxation (antispasmodic). More selective for smooth muscle than papaverine; no anticholinergic activity. |
| Clinical Uses | Smooth muscle spasms: biliary colic, renal colic, ureteral colic, intestinal/colonic spasm, dysmenorrhea, uterine spasm in labor |
| Adverse Effects | Dizziness, headache, hypotension, nausea, tachycardia, palpitations (generally well tolerated) |
| Contraindications | Severe hepatic/renal/cardiac failure, hypotension, hypersensitivity; caution in hypotension |
| MOA | Provides ionized calcium (Ca²⁺) → membrane stabilization (cardiac myocytes); counteracts hyperkalemia by stabilizing cardiac membrane potential; activates enzyme systems; required for coagulation cascade |
| Clinical Uses | Hypocalcemia, hyperkalemia (cardiac protection — does NOT lower K⁺), hypocalcemic tetany, magnesium toxicity antidote, citrate toxicity (massive transfusion), black widow spider envenomation |
| Adverse Effects | Bradycardia/cardiac arrest if given too fast IV, hypercalcemia, tissue necrosis if extravasation occurs, flushing, nausea |
| Contraindications | Hypercalcemia, ventricular fibrillation, digoxin toxicity (↑ risk of arrhythmia), concurrent thiazide diuretics (risk of hypercalcemia) |
| MOA | Precursor to glutathione → replenishes glutathione stores → antioxidant; also mucolytic (cleaves disulfide bonds in mucus glycoproteins → reduces viscosity); in paracetamol overdose, regenerates glutathione to detoxify NAPQI |
| Clinical Uses | Mucolytic (COPD, cystic fibrosis, bronchiectasis), paracetamol/acetaminophen overdose (gold standard antidote), contrast-induced nephropathy prevention, hepatic failure |
| Adverse Effects | Nausea, vomiting, rash, anaphylactoid reaction (IV infusion — flushing, bronchospasm, urticaria), unpleasant odor |
| Contraindications | Hypersensitivity to NAC; caution in asthma (may precipitate bronchospasm — especially IV) |
| MOA | D2 receptor antagonist (central & peripheral) + 5-HT4 agonist → ↑ gastric motility and gastric emptying, ↑ lower esophageal sphincter tone, central antiemetic (blocks CTZ dopamine receptors) |
| Clinical Uses | Nausea & vomiting (post-op, chemo, gastroparesis), gastroesophageal reflux, diabetic gastroparesis, as prokinetic agent |
| Adverse Effects | Tardive dyskinesia (long-term use — irreversible), acute dystonia/extrapyramidal reactions, akathisia, Parkinsonism, hyperprolactinemia (galactorrhea, amenorrhea), drowsiness |
| Contraindications | GI obstruction/perforation, pheochromocytoma, Parkinson's disease, history of tardive dyskinesia, epilepsy, concurrent dopamine agonists; avoid >3 months (tardive dyskinesia risk) |
| MOA | Cyproheptadine: first-gen H1 antihistamine + serotonin (5-HT2) antagonist → appetite stimulation (blocks serotonin-mediated satiety signals) + antiallergic effects. B-vitamins (B1, B2, B6, B12): cofactors in metabolism. Lysine: essential amino acid for protein synthesis. |
| Clinical Uses | Poor appetite/anorexia, failure to thrive, weight gain stimulation, allergic conditions (rhinitis, urticaria), prevention of migraines |
| Adverse Effects | Drowsiness, sedation, dry mouth, urinary retention, constipation, weight gain, dizziness |
| Contraindications | Glaucoma, BPH/urinary retention, asthma/COPD (may thicken secretions), MAOIs, neonates/premature infants, elderly (increased CNS effects) |
| MOA | Prodrug → activated by CYP2C19 in liver → active metabolite irreversibly binds P2Y12 ADP receptor on platelets → inhibits ADP-induced platelet aggregation (irreversible for platelet's lifetime ~7–10 days) |
| Clinical Uses | ACS (with or without PCI), ischemic stroke/TIA, peripheral arterial disease; dual antiplatelet therapy (DAPT) with aspirin post-stent |
| Adverse Effects | Bleeding (major concern), GI bleeding, TTP (rare but serious), rash, neutropenia, bruising |
| Contraindications | Active bleeding, peptic ulcer, intracranial hemorrhage, severe hepatic impairment (impaired prodrug activation), CYP2C19 poor metabolizers (reduced efficacy), concomitant strong CYP2C19 inhibitors (e.g., omeprazole — reduces efficacy) |
| MOA | Non-selective β1 + β2 blocker + α1 blocker → negative chronotropy/inotropy (β) + vasodilation (α1 blockade) + antioxidant properties. No intrinsic sympathomimetic activity. |
| Clinical Uses | Heart failure with reduced EF (HFrEF) — reduces mortality, hypertension, post-MI LV dysfunction, stable angina |
| Adverse Effects | Bradycardia, hypotension, dizziness, fatigue, worsening HF on initiation, bronchospasm (β2 blockade), hyperglycemia masking, peripheral coldness, fluid retention |
| Contraindications | Acute decompensated HF, severe bradycardia/heart block (2nd/3rd degree), cardiogenic shock, severe asthma/COPD, sick sinus syndrome without pacemaker |
| MOA | Competitive aldosterone receptor antagonist in collecting tubules → blocks Na⁺/K⁺ exchange → natriuresis + K⁺ sparing. Also has anti-androgenic properties (weak). |
| Clinical Uses | Heart failure (HFrEF) — reduces mortality, hyperaldosteronism (primary & secondary), hypertension, ascites in cirrhosis, edema, female-pattern hair loss, PCOS |
| Adverse Effects | Hyperkalemia (most dangerous), gynecomastia/breast tenderness (males), menstrual irregularities, GI upset, metabolic acidosis |
| Contraindications | Hyperkalemia, severe renal failure (eGFR <30), Addison's disease, concurrent use of other K⁺-sparing agents or ACE inhibitors (risk of dangerous hyperkalemia), anuria |
| MOA | Carbapenem β-lactam antibiotic → binds penicillin-binding proteins (PBPs) → inhibits bacterial cell wall synthesis (transpeptidation of peptidoglycan) → bactericidal. Resistant to most β-lactamases including ESBLs. |
| Clinical Uses | Severe/life-threatening infections: hospital-acquired pneumonia, septicemia, intra-abdominal infections, meningitis, febrile neutropenia, complicated UTIs, Pseudomonas infections |
| Adverse Effects | GI upset (nausea, diarrhea), C. difficile colitis, hypersensitivity reactions, seizures (less than imipenem), thrombophlebitis at injection site, elevated LFTs |
| Contraindications | Hypersensitivity to carbapenems; caution with penicillin allergy (cross-reactivity ~1%); reduces valproate levels (avoid combination — risk of seizures) |
| MOA | Proton Pump Inhibitor (PPI) → prodrug activated in acidic environment → irreversibly inhibits H⁺/K⁺-ATPase (proton pump) on gastric parietal cells → profound, long-lasting suppression of gastric acid secretion |
| Clinical Uses | GERD, peptic ulcer disease, H. pylori eradication (triple therapy), Zollinger-Ellison syndrome, NSAID-induced ulcer prevention, stress ulcer prophylaxis, erosive esophagitis |
| Adverse Effects | Headache, GI upset, hypomagnesemia (long-term), ↓ B12 absorption (long-term), C. difficile risk (long-term), osteoporosis/fractures (long-term), CYP2C19 inhibition (↓ clopidogrel efficacy) |
| Contraindications | Hypersensitivity; caution with clopidogrel (reduces antiplatelet efficacy); note: this patient is on both! Consider switching to pantoprazole. |
| MOA | Loop diuretic → inhibits Na⁺/K⁺/2Cl⁻ cotransporter (NKCC2) in the thick ascending limb of Loop of Henle → massive natriuresis and diuresis; also causes venodilation (reduces preload acutely) |
| Clinical Uses | Acute pulmonary edema, chronic heart failure, hypertension, edema (hepatic, renal, cardiac), hypercalcemia, hyperkalemia (adjunct), ascites |
| Adverse Effects | Hypokalemia, hyponatremia, hypomagnesemia, metabolic alkalosis, dehydration, ototoxicity (high doses/IV), hyperuricemia (gout), hyperglycemia, hypocalcemia |
| Contraindications | Anuria/severe oliguria, sulfonamide hypersensitivity, hepatic coma, severe hypokalemia/hyponatremia, pre-coma states in hepatic cirrhosis |
| MOA | Exogenous colloid → ↑ oncotic pressure in plasma → expands intravascular volume; also binds and transports drugs, hormones, fatty acids; maintains vascular integrity |
| Clinical Uses | Hypoalbuminemia, cirrhotic ascites (post-paracentesis albumin replacement), spontaneous bacterial peritonitis (SBP prophylaxis), hepatorenal syndrome, burns, nephrotic syndrome, hypovolemic shock |
| Adverse Effects | Fluid overload/pulmonary edema (if given too fast/too much), anaphylactic reactions, fever, chills, hypotension, risk of volume overload in cardiac/renal disease |
| Contraindications | Cardiac failure with fluid overload, severe anemia, pulmonary edema, hypersensitivity to albumin products |
| MOA | Combination of diphenhydramine (H1 antihistamine) + 8-chlorotheophylline → blocks H1 receptors in vestibular nucleus and vomiting center (CTZ) + anticholinergic (muscarinic) blockade → antiemetic and anti-vertigo |
| Clinical Uses | Motion sickness (prevention & treatment), nausea & vomiting, vertigo, Ménière's disease, post-op nausea |
| Adverse Effects | Sedation/drowsiness (main effect), dry mouth, blurred vision, urinary retention, constipation, paradoxical excitation (in children) |
| Contraindications | Glaucoma, BPH, epilepsy, porphyria, neonates/premature infants, concurrent MAOI therapy, severe hepatic disease |
| MOA | Highly negatively charged polysaccharide → binds antithrombin III (AT-III) → conformational change in AT-III → 1000× acceleration of AT-III's inhibition of thrombin (IIa), Factor Xa, IXa, XIa, XIIa → anticoagulation |
| Clinical Uses | DVT/PE (treatment & prophylaxis), ACS, cardiopulmonary bypass, hemodialysis circuit anticoagulation, disseminated intravascular coagulation (DIC), VTE prophylaxis (low-dose SC) |
| Adverse Effects | Bleeding, Heparin-Induced Thrombocytopenia (HIT) — type I (mild, non-immune) and type II (immune-mediated, paradoxical thrombosis — serious), osteoporosis (long-term), hyperkalemia (↓ aldosterone), hypertransaminasemia |
| Contraindications | Active major bleeding, HIT (type II), hypersensitivity, severe thrombocytopenia, intracranial hemorrhage; caution in severe hypertension, recent surgery |
| Antidote | Protamine sulfate (reverses unfractionated heparin) |
| MOA | Isotonic crystalloid solution → distributes into extracellular fluid (intravascular + interstitial); expands plasma volume; does not significantly shift fluid into cells |
| Clinical Uses | IV fluid resuscitation, hypovolemia, hyponatremia (symptomatic), maintenance IV fluid, drug dilution/infusion vehicle, metabolic alkalosis replacement |
| Adverse Effects | Hyperchloremic metabolic acidosis (large volumes), fluid overload, hypertension, dilutional hyponatremia (if used inappropriately), edema |
| Contraindications | Hypernatremia, hyperchloremia, congestive heart failure (use cautiously), conditions requiring fluid restriction |
Clopidogrel (Lowplat) + Omeprazole (Risek): Omeprazole inhibits CYP2C19, which is required to activate clopidogrel to its active metabolite. This reduces clopidogrel's antiplatelet efficacy. Consider switching to Pantoprazole (weaker CYP2C19 inhibitor) if PPI is needed alongside clopidogrel.Heparin + Aspirin + Clopidogrel (Triple therapy): Significantly ↑ bleeding risk — monitor closely.Tramadol + any serotonergic drug: Risk of serotonin syndrome — review full drug list.