Molecular structure pattern

Heavy Menstrual Bleeding Drug Summary

Antigonadotropin

Drug Dosage Remarks
Danazol 200 mg PO 24 hourly for 12 weeks Adverse Reactions
  • CV effects (hypertension, edema, flushing); CNS effects (depression, dizziness, headache, sleep disorder); Dermatologic effects (acne, alopecia, mild hirsutism, rash); Endocrine effects (amenorrhea, decreased breast size, clitoris hypertrophy, increased LDL, menstrual disturbances); GI effects (nausea/vomiting, weight gain, constipation); GU effects (vaginal dryness or irritation, pelvic pain); Hematologic effects (eosinophilia, leukocytosis, leukopenia); Other effects (hepatic adenoma, paresthesia, hematuria, voice change)
Special Instructions
  • Use with caution in patients with diabetes mellitus (DM) or diseases exacerbated by fluid retention (eg asthma, epilepsy, migraine, cardiac or renal disease)
  • Avoid in patients with undiagnosed vaginal bleeding, porphyria, severe hepatic, renal or cardiac impairment, pregnancy, breastfeeding

Haemostatics

Drug Dosage Remarks
Ethamsylate 500 mg PO 6 hourly from start of bleeding until menstruation ceases Adverse Reactions
  • Other effects (headache, skin rashes, nausea)
Special Instructions
  • Avoid in pregnant patients, in patients with hypersensitivity, porphyria
Tranexamic acid 1 g PO 6-8 hourly starting at day 1 of menses for up to 5 days Adverse Reactions
  • CNS effects (headache, migraine); GI effect (abdominal pain); Musculoskeletal effects (back pain, muscle pain, arthralgia); Respiratory effect (nasal symptoms); Hematologic effect (anemia); Other effect (fatigue)
Special Instructions
  • Use with caution in patients with upper urinary tract bleeding or obstruction due to clot formation, disseminated intravascular coagulation, renal impairment, subarachnoid hemorrhage, in patients receiving hormonal contraceptives or Tretinoin
  • Avoid use in patients who are at risk of or with previous or active thromboembolic disease (eg hypercoagulopathy, retinal artery occlusion, cerebral thrombosis, deep vein thrombosis [DVT], pulmonary embolism)

Nonsteroidal Anti-inflammatory Drugs (NSAIDs)

Drug Dosage Remarks
Anthranilic Acid Derivative Adverse Reactions
  • GI effects (abdominal cramps, heartburn, indigestion, nausea/vomiting, gastric or duodenal ulcers, gastritis); Hematologic effect (bleeding); Hepatic effect (increased LFT); CNS effects (headache, nervousness, dizziness); Other rare effects (hypertension, tachycardia, urticaria, anaphylactic reactions, dyspnea, allergic rhinitis, hyperkalemia, tinnitus)
Special Instructions
  • Should be taken with food
  • Use with caution in patients requiring mental alertness in performing tasks (eg driving or operating machineries), patients with coagulation disorders, hepatic impairment, hypertension, patients receiving anticoagulants or other agents causing hyperkalemia (eg ACE inhibitors)
  • Avoid in patients allergic to Aspirin or other NSAIDs, patients with active ulceration or chronic inflammation of the GI tract, patients with renal impairment, or in perioperative pain in the setting of coronary artery bypass graft (CABG) surgery
    • Associated with increased risk of myocardial infarction (MI) and stroke following CABG surgery
  • Withhold use for 8-12 hours (4-6 half-lives) prior to surgical or dental procedures
Mefenamic acid 250-500 mg PO 8 hourly beginning with onset of menses and continuing for 5 days or until cessation of flow
Propionic Acid Derivative
Naproxen 825-1,375 mg/day PO divided 12 hourly

Progestogens

Drug Dosage Remarks
Levonorgestrel 1 IUS unit inserted into the uterine cavity within 7 days of the onset of menstruation Adverse Reactions
  • CNS effects (headache, depression); Endocrine effects (amenorrhea after 1 year of use, enlarged follicles, breast pain/tenderness); GI effect (abdominal pain); Dermatologic effect (acne); GU effects (uterine/vaginal bleeding/spotting, pelvic pain); Other effects (ectopic pregnancy, intrauterine device [IUD] expulsion)
Special Instructions
  • Use with caution in patients with DM, coagulopathy, congenital or other heart disease, history of ectopic pregnancy, in patients receiving anticoagulants
  • Avoid in patients with uterine anomaly, acute pelvic inflammatory disease (PID), history of PID, uterine or cervical neoplasia, untreated cervicitis or vaginitis, unremoved IUD, undiagnosed AUB, active hepatic disease, breast cancer, pregnancy
  • Postpartum insertion should be postponed until 6 weeks after delivery
Lynestrenol 10 mg PO 24 hourly for 10 days Adverse Reactions
  • CV effects (fluid retention, edema); CNS effects (depression, migraine); Dermatologic effects (urticaria, rash); Endocrine effects (gynecomastia, menstrual flow changes, breast tenderness, change in libido); GI effects (change in weight/appetite); Other effects (LFT/lipid profile changes, anaphylactic reactions)
Special Instructions
  • Use with caution in patients with DM, hypertension, migraine, depression, diseases exacerbated by fluid retention (eg asthma, epilepsy, migraine, cardiac or renal disease)
  • Avoid use in patients with history or active thromboembolic disorders, hepatic disease, breast cancer, undiagnosed vaginal bleeding, pregnancy
Medroxyprogesterone 2.5-10 mg PO 24 hourly for 5-10 days starting on the sixteenth day of menstrual cycle Adverse Reactions
  • CNS effects (depression, dizziness, headache); Endocrine effects (irregular menses, decreased libido); GI effects (abdominal pain, weight gain); CV effect (edema); Dermatologic effects (acne, rash); Other effects (dysmenorrhea, vaginitis, arthralgia, bone mineral loss, anaphylactic reactions, ectopic pregnancy)
Special Instructions
  • Use with caution in patients with DM, depression, diseases exacerbated by fluid retention (eg asthma, epilepsy, migraine, cardiac or renal disease)
  • Avoid use in patients with history or active thromboembolic disorders, cerebrovascular disease, hepatic disease, breast cancer, undiagnosed vaginal bleeding, pregnancy
Nomegestrol acetate 5 mg PO 24 hourly from sixteenth to twenty-fifth day of cycle Adverse Reactions
  • Endocrine effects (modification of menstruation, amenorrhea, intercurrent bleeding); Other effects (weight gain, insomnia)
Special Instructions
  • Use with caution in patients with history of MI, cerebrovascular diseases, hypertension, DM, predisposition to thromboembolism
  • Avoid in patients with thrombophlebitis, liver dysfunction, undiagnosed genital hemorrhage
Norethisterone
(Norethindrone)
10-15 mg/day PO divided 8 hourly for 10 days, in a cyclical regimen Adverse Reactions
  • CV effects (cerebral embolism, DVT, edema); CNS effects (depression, dizziness, migraine, mood swings); Dermatologic effects (acne, chloasma, rash); Endocrine effects (amenorrhea, menstrual flow changes, breast tenderness); GI effects (nausea, weight gain/loss); Other effects (LFT abnormalities, pulmonary embolism, anaphylactic reactions)
Special Instructions
  • Use with caution in patients with DM, hyperlipidemias, high risk of thromboembolism, depression, diseases exacerbated by fluid retention (eg asthma, epilepsy, migraine, cardiac or renal disease)
  • Avoid use in patients with history or active thromboembolic disorders, hepatic disease, breast cancer, undiagnosed vaginal bleeding, pregnancy
 
 

Progestogen & Estrogen Combinations

Drug Dosage Remarks
Dienogest/estradiol
valerate
1 tab PO 24 hourly starting on day 1 of menses for 28 days Adverse Reactions
  • CV effects (edema, varicose vein aggravation); CNS effects (depression, migraine, mood swings); Dermatologic effects (chloasma, rash); Endocrine effects (amenorrhea, menstrual flow changes, breast tenderness, spotting); GI effects (bloating, abdominal cramps, nausea/vomiting, weight change); GU effects (endocervical hyperplasia, fibroid enlargement, vaginal candidiasis); Hematologic effects (decreased folate, porphyria exacerbation); Other effects (contact lens intolerance, rhinitis, anaphylactic reactions, systemic lupus erythematosus [SLE] exacerbation)
  • Associated with arterial thromboembolism, cerebral hemorrhage, cerebral thrombosis, hypertension, MI, venous thrombosis, gallbladder disease, hepatic adenomas, retinal thrombosis, pulmonary embolism
Special Instructions
  • Use with caution in patients with DM, familial defects of lipoprotein metabolism, high risk of thromboembolism, depression, diseases exacerbated by fluid retention (eg asthma, epilepsy, migraine, cardiac or renal disease)
  • Avoid use in patients with history or active thromboembolic disorders, cerebrovascular disease, coronary artery disease, valvular heart disease, uncontrolled hypertension, thrombophilias, DM with vascular involvement, severe headache with focal neurological symptoms, migraine, hepatic disease, breast or endometrial cancer, smoking ≥15 cigarettes/day, pregnancy
Levonorgestrel/ethinyl estradiol1 1 tab PO 24 hourly starting on day 1 of menses for 21 days
1Combination with Ferrous fumarate is available. Please see the latest MIMS for specific formulations and prescribing information.

Disclaimer

All dosage recommendations are for non-elderly adults with normal renal and hepatic function unless otherwise stated. 
Not all products are available or approved for above use in all countries. 
Products listed in the Drug Summary are based on indications stated in the locally approved product monographs. 
Please refer to local product monographs in Related MIMS Drugs for country-specific prescribing information.