Psoriasis Drug Summary

Last updated: 24 June 2025

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Calcineurin Inhibitors


Drug Available Strength Dosage Remarks
Pimecrolimus 1% cream

Apply thinly to affected skin 12 hourly

Adverse Reactions

  • Local effects: Burning, sensation of warmth which usually decreases with continued use, application site reactions (eg irritation, erythema, itching)
  • Less common: Bacterial and viral infections
  • If lymphadenopathy occurs, the cause should be investigated and if no clear cause, Pimecrolimus should be discontinued
Special Instructions
  • Contraindicated in patients with malignant or premalignant skin lesions and areas affected by acute cutaneous viral infections or in immunocompromised patients
    • Clinical cutaneous infections should be cleared before application of Pimecrolimus
  • Use is not recommended in patients with Netherton’s syndrome or skin conditions which may increase the potential for systemic absorption
  • Avoid excessive or unnecessary exposure to UV light and sunlight during treatment
    • Higher dose than used in humans shortened time to skin tumor formation in an animal photocarcinogenicity study
  • Should not be used with occlusive dressing
  • Patients should minimize or avoid natural or artificial sunlight
Tacrolimus 0.03% ointment
0.1% ointment

Apply thinly to affected skin 12 hourly

Cytotoxic Chemotherapy


Drug Dosage Remarks
Hydroxycarbamide
(Hydroxyurea)
500 mg PO 8-24 hourly Adverse Reactions
  • Hematologic effect (bone marrow suppression); GI effects (nausea/vomiting); Hepatic effect (mild hepatitis which is not permanent); CNS effects (dizziness, drowsiness, disorientation, hallucinations, convulsions, headache); Dermatologic effects (hyperpigmentation, transient alopecia, cutaneous vasculitic toxicities); Other effects (renal function impairment, dyspnea, hyperuricemia)
Special Instructions
  • Contraindicated in patients with severe bone marrow depression, severe anemia, pregnancy and lactation
  • Use with caution in patients with renal impairment
  • Vaccination with live-virus vaccines not recommended
  • Monitor CBC with platelets, uric acid, hepatic and renal function regularly prior to and during treatment
    • Toxic range: Hb <4.5 g/dL, neutrophils <2,000 cells/mm3, platelet count <80,000 mm3
  • Discontinue therapy if there is infection and if no response after 8 weeks of treatment
Methotrexate 7.5-25 mg PO/IV/IM once weekly
Max dose:
30 mg/wk or
2.5 mg PO 12 hourly x 3 doses or 8 hourly x 4 doses given weekly
May increase dosage gradually by 2.5 mg/week
Max dose: 30 mg/week or
2.5 mg PO 24 hourly for 5 days followed by rest period for ≥2 days
Max dose: 6.25 mg/day or
10-25 mg SC once weekly
Max dose: 25-30 mg/week
Adverse Reactions
  • Hematologic effects (bone marrow depression which can occur abruptly, leukopenia, thrombocytopenia, anemia); GI effects (nausea/vomiting, loss of appetite, abdominal pain, diarrhea); Hepatic effect (acute and chronic liver damage); CNS effects (dizziness, fever, seizure); Other effects (renal failure, renal tubular necrosis, interstitial lung disease, potentially fatal dermatologic reactions eg toxic epidermal necrolysis and Stevens-Johnson syndrome, ocular irritation, alopecia, osteoporosis, neurotoxicity, impaired fertility, arthralgia, soft tissue and bone necrosis)
  • Low-dose Methotrexate has been associated with development of malignant lymphomas
  • Use may predispose patients to opportunistic infection
  • Early signs of toxicity: Mouth ulcers, stomatitis, diarrhea. If these occur, therapy may need to be interrupted
Special Instructions
  • Avoid in patients with alcoholic liver disease or abnormal LFT or in those with significant renal impairment, blood disorders or immunodeficiency
  • Contraindicated in pregnancy and lactation
  • Use with caution in patients with peptic ulcer disease, ulcerative colitis, hepatic or renal impairment
  • Monitor CBC with platelets, LFT and renal function prior to and regularly during therapy
  • Baseline liver biopsy should be performed before Methotrexate institution in patients with risk factors for hepatotoxicity
  • Medication should be interrupted if diarrhea, myelosuppression, stomatitis or signs of liver dysfunction occur
  • Signs of infection (eg fever, sore throat) should be reported to physician immediately
  • May cause folic acid deficiency, consider giving folate supplement

Warts & Calluses Preparations*


Drug Available Strength Dosage Remarks
Salicylic acid 2-11.8% cream, lotion, ointment, shampoo

Apply 6-24 hourly

Adverse Reactions

  • Prolonged use over large BSA may result in salicylate toxicity
  • Local irritation when in contact with normal skin, sensitivity, excessive drying
Special Instructions
  • Avoid use on broken skin, mouth, eyes, mucous membranes and anogenital regions
Sulfur 10% ointment

Apply 12-24 hourly

Adverse Reactions

  • Skin irritation and dermatitis
Special Instructions
  • Avoid contact with eyes, mouth and other mucous membranes
Urea 10% cream, lotion
20% cream

Apply 8-12 hourly

Adverse Reactions

  • May be irritating to sensitive skin
Special Instructions
  • Avoid contact with eyes
  • Contraindicated in patients with viral skin infection
*Warts and calluses preparations combined with a number of different agents are available. Please see the latest MIMS for specific formulations and prescribing information.

Disclaimer

All dosage recommendations are for non-pregnant and non-breastfeeding women and 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.  

Related MIMS Drugs