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A comprehensive set of vocabulary flashcards covering major hormones, drugs, mechanisms, indications, contraindications, and adverse effects discussed in the lecture on women's health, men's health, and antineoplastic pharmacology.
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Estrogens
Female sex steroid hormones responsible for development and maintenance of the reproductive system and secondary sex characteristics.
Progesterone
Female sex steroid hormone that prepares the uterus for implantation and maintains pregnancy.
Follicle-Stimulating Hormone (FSH)
Pituitary gonadotropin that stimulates ovarian follicle growth and estradiol production.
Luteinizing Hormone (LH)
Pituitary hormone that triggers ovulation and supports corpus luteum function.
Estradiol
Principal and most active endogenous estrogen synthesized in ovarian follicles.
Estrone
One of the three major endogenous estrogens, less potent than estradiol.
Estriol
Weak endogenous estrogen, predominant during pregnancy.
Conjugated Estrogens (Premarin)
Steroidal mixture of natural estrogens used for estrogen-replacement therapy.
Diethylstilbestrol
Nonsteroidal synthetic estrogen no longer marketed in the United States due to safety concerns.
Hormone Replacement Therapy (HRT)
Use of estrogen (often with progestin) to relieve menopausal symptoms; not recommended for osteoporosis prevention alone.
Estrogen Indications
Treatment of estrogen deficiency states, contraception (with progestin), menopausal vasomotor symptoms, osteoporosis prophylaxis, certain cancers.
Estrogen Contraindications
Estrogen-dependent cancer, undiagnosed vaginal bleeding, pregnancy, active or past thromboembolic events, allergy.
Thrombolytic Events
Most serious adverse effect associated with estrogen therapy, includes DVT, PE, and stroke.
Chloasma
Patchy facial hyperpigmentation that may occur with estrogen use and sun exposure.
Progestins
Synthetic progesterone-like drugs such as medroxyprogesterone, norethindrone, and levonorgestrel.
Medroxyprogesterone (Provera)
Progestin used for uterine bleeding, amenorrhea, endometrial cancer, renal cancer, and contraception.
Megestrol (Megace)
Oral progestin used as appetite stimulant in AIDS/cancer and for palliative breast cancer management.
Progestin Mechanism
Induces secretory endometrium, thickens cervical mucus, inhibits pituitary gonadotropins, relaxes uterine muscle.
Monophasic Oral Contraceptive
Pill pack delivering constant estrogen-progestin dose each active day.
Triphasic Oral Contraceptive
Pill whose hormone levels vary in three distinct phases to mimic natural cycle.
Contraceptive Mechanism
Inhibits gonadotropin release, prevents ovulation, thickens cervical mucus, may inhibit implantation.
Contraceptive Contraindications
Pregnancy, high risk or history of thromboembolism, hormone-sensitive cancer, severe hypertension.
Bisphosphonates
Osteoporosis drugs that inhibit osteoclast-mediated bone resorption (e.g., alendronate).
Alendronate (Fosamax)
First non-hormonal oral bisphosphonate for osteoporosis; taken with water, remain upright 30 min.
Selective Estrogen Receptor Modulators (SERMs)
Drugs like raloxifene that stimulate estrogen receptors on bone while blocking them in breast/uterus.
Raloxifene (Evista)
SERM used to prevent postmenopausal osteoporosis; may cause hot flashes and VTE risk.
Calcitonin (Calcimar)
Hormone drug that directly inhibits osteoclastic bone resorption; used for osteoporosis.
Teriparatide (Forteo)
Recombinant PTH analogue that stimulates new bone formation; daily SC injection.
Denosumab (Prolia)
Monoclonal antibody that blocks osteoclast activation; SC every 6 months with calcium/vit D.
Romosozumab (Evenity)
New sclerostin-inhibiting antibody for osteoporosis treatment.
Clomiphene (Clomid)
Nonsteroidal ovulation stimulant that blocks estrogen receptors, increasing FSH/LH release.
Menotropins
Combination of FSH and LH used to stimulate ovarian follicle development or spermatogenesis.
Chorionic Gonadotropin Alfa (Ovidrel)
Recombinant hCG used to trigger ovulation and support corpus luteum.
Oxytocin (Pitocin)
Uterine stimulant used to induce or augment labor and control postpartum bleeding.
Dinoprostone
Prostaglandin used for cervical ripening and labor induction.
Methylergonovine (Methergine)
Ergot alkaloid that increases uterine tone to prevent postpartum hemorrhage.
Mifepristone (Mifeprex)
Progesterone antagonist used with prostaglandin for medical abortion.
Tocolytics
Uterine relaxants like indomethacin or nifedipine used to halt premature labor.
Soy (Estrasorb)
Herbal product with estrogen-like compounds for menopausal symptom relief; applied topically.
Saw Palmetto
Herbal product used for BPH and alopecia; may interact with NSAIDs like ibuprofen.
Androgens
Male sex hormones such as testosterone responsible for male sexual development and anabolic effects.
Testosterone
Primary endogenous androgen; available in depot injection, patches, and gels.
Anabolic Steroids
Synthetic derivatives of testosterone with tissue-building properties; Schedule III abuse risk.
Danazol (Danocrine)
Synthetic androgen used for hereditary angioedema, endometriosis, and fibrocystic breast disease.
5-Alpha Reductase Inhibitors
Finasteride and dutasteride; reduce prostate size by inhibiting conversion of testosterone to DHT.
Finasteride
5-Alpha reductase inhibitor for BPH and male pattern baldness; teratogenic to women handling tablets.
Alpha1-Adrenergic Blockers
Drugs like tamsulosin that relax prostatic smooth muscle for BPH symptom relief.
Androgen Receptor Blockers
Agents such as flutamide that block testosterone at prostate receptors; used for prostate cancer.
GnRH Analogues
Leuprolide, goserelin; decrease testosterone by down-regulating pituitary gonadotropins.
PDE5 Inhibitors
Sildenafil, tadalafil, etc.; increase cGMP to treat erectile dysfunction; contraindicated with nitrates.
Alprostadil (Caverject)
Prostaglandin injected into corpus cavernosum or urethra for ED.
Priapism
Prolonged, painful erection; medical emergency linked to ED drugs or androgen therapy.
Peliosis Hepatis
Blood-filled liver cysts associated with long-term anabolic steroid use.
Cancer
Malignant uncontrolled cellular growth capable of invasion and metastasis.
Primary Lesion
Original site of malignant tumor development.
Metastasis
Spread of cancer cells to distant body sites forming secondary tumors.
Paraneoplastic Syndrome
Group of symptoms (e.g., cachexia) not directly related to tumor invasion but caused by cancer.
Cell Cycle
Series of phases (G0, G1, S, G2, M) through which a cell passes to divide.
Cell Cycle-Specific (CCS) Drugs
Antineoplastics that act during a particular phase of the cell cycle (e.g., antimetabolites).
Cell Cycle-Nonspecific (CCNS) Drugs
Agents cytotoxic in any cell-cycle phase (e.g., alkylating drugs, anthracyclines).
Antimetabolites
CCS drugs (e.g., methotrexate, 5-FU) that mimic metabolites, inhibiting DNA/RNA synthesis in S phase.
Methotrexate (MTX)
Folate antagonist antimetabolite used for cancers, severe psoriasis, and rheumatoid arthritis.
Leucovorin Rescue
Administration of folinic acid to reduce methotrexate-induced bone marrow suppression.
Purine Antagonists
Antimetabolites like mercaptopurine that disrupt purine nucleotide pathways.
Pyrimidine Antagonists
Agents such as fluorouracil that inhibit pyrimidine metabolism and DNA synthesis.
Tumor Lysis Syndrome
Metabolic emergency after rapid tumor cell destruction causing hyperuricemia, hyperkalemia, etc.
Mitotic Inhibitors
Vinca alkaloids and taxanes that disrupt microtubules, blocking mitosis.
Vincristine
Vinca alkaloid notable for neurotoxicity; fatal if given intrathecally.
Paclitaxel
Taxane mitotic inhibitor derived from yew tree used for breast, ovarian, lung cancers.
Topoisomerase I Inhibitors
Camptothecin derivatives (irinotecan, topotecan) that prevent DNA religation during replication.
Topoisomerase II Inhibitors
Etoposide class drugs used for testicular and small-cell lung cancer.
Asparaginase
Antineoplastic enzyme that deprives leukemia cells of asparagine, causing cell death.
Alkylating Agents
CCNS drugs (e.g., cyclophosphamide, cisplatin) that add alkyl groups to DNA, preventing replication.
Cisplatin
Platinum-based alkylator for solid tumors; nephrotoxic and ototoxic.
Cyclophosphamide
Nitrogen mustard alkylator for hematologic and solid tumors; prodrug activated in liver.
Cytotoxic Antibiotics
Anthracyclines and others that intercalate DNA; examples include doxorubicin and bleomycin.
Doxorubicin
Anthracycline causing dose-related cardiomyopathy; dexrazoxane used for cardioprotection.
Bleomycin
Cytotoxic antibiotic notable for pulmonary fibrosis rather than bone marrow suppression.
Bevacizumab (Avastin)
Monoclonal antibody angiogenesis inhibitor that blocks tumor blood vessel formation.
Imatinib (Gleevec)
Tyrosine kinase inhibitor targeting BCR-ABL in chronic myeloid leukemia.
Hydroxyurea
Ribonucleotide reductase inhibitor used for CML and squamous cell carcinoma.
Mitotane (Lysodren)
Adrenal cytotoxic drug for inoperable adrenal cortex carcinoma.
Octreotide (Sandostatin)
Somatostatin analogue managing carcinoid crisis and VIPoma diarrhea.
Extravasation
Leakage of vesicant chemotherapy into tissues causing severe local damage.
Nadir
Lowest point of blood cell counts after chemotherapy, indicating maximum bone marrow suppression.
Myelosuppression
Suppression of bone marrow activity leading to anemia, leukopenia, thrombocytopenia.
Emetic Potential
Likelihood that a drug will cause nausea and vomiting.
Cytoprotective Agents
Drugs like amifostine or dexrazoxane given to reduce specific chemotherapy toxicities.
Hand-Foot Syndrome
Palmar-plantar dysesthesia seen with agents like capecitabine presenting as painful redness/swelling.
Pelvic Osteonecrosis of Jaw
Serious complication associated with bisphosphonates, particularly IV formulations.
Phototoxicity
Skin reaction induced by light exposure after certain drug use (e.g., estrogens).
Vena Thromboembolism (VTE)
Serious SERM adverse effect involving deep vein or pulmonary clots.
Hypercalcemia
Elevated serum calcium; may occur as paraneoplastic syndrome or adverse effect of teriparatide.
Hepatic First-Pass Effect
Extensive metabolism of oral drugs (e.g., testosterone) in the liver before systemic circulation.
Schedule III Drugs
Controlled substances with moderate abuse potential, includes anabolic steroids.
Peliosis
Formation of blood-filled cysts in the liver linked to anabolic steroid therapy.
Gynecomastia
Male breast enlargement, possible adverse effect of finasteride or androgen imbalance.
Sclerostin Inhibitor
Drug class blocking sclerostin to stimulate bone formation (e.g., romosozumab).
Cholinergic Diarrhea
Severe early-onset diarrhea characteristic of irinotecan therapy.
Dexrazoxane
Cardioprotective agent given with doxorubicin; also used for anthracycline extravasation.