SOLODYN (minocycline 24 hour)
SELF ADMINISTRATION - ORAL
Indications for Prior Authorization:
- Acne vulgaris
All of the following must be met as a condition for coverage (must include chart note documentation as supporting information):
- Patient must have tried/failed generic minocycline AND generic doxycycline, with chart note support of reason for treatment failures (i.e., gastrointestinal side effects); note treatment failure due to ineffectiveness of minocycline or doxycycline is not considered towards Solodyn prior authorization approval
- Must be prescribed/consulted by a dermatologist
- Current weight is required
This Medication is Not Approvable for the following condition(s):
- Any condition not listed above as an approved indication
The extended release product (Solodyn) is not FDA indicated for the following:
- Acute intestinal amebiasis
- Actinomycosis
- Anthrax
- Asymptomatic carriers of Neisseria meningitidis/li>
- Campylobacter
- Cholera
- Clostridium
- Gram-negative infections
- Listeriosis
- Mycobacterial infection
- Ophthalmic infections
- Relapsing fever
- Respiratory tract infections
- Rickettsial infections
- Sexually transmitted diseases
- Skin and skin structure infections>
- Urinary tract infections
- Vincent infection
- Yaws>
- Zoonotic infections
Dosing:
Extended release
- Acne (inflammatory, non-nodular, moderate to severe): 1 mg/kg once daily for 12 weeks
- Higher doses have not shown to be of additional benefit and may be associated with more acute vestibular adverse reactions
Minocycline ERa (Solodyn) Tablets Dosing | ||||||||
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45 to 49 kg
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45 mg
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1 to 0.92 mg/kg
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50 to 59 kg
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55 mg
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1.1 to 0.93 mg/kg
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60 to 71 kg
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65 mg
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1.08 to 0.92 mg/kg
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72 to 84 kg
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80 mg
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1.11 to 0.95 mg/kg
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85 to 96 kg
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90 mg
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1.06 to 0.94 mg/kg
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97 to 110 kg
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105 mg
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1.08 to 0.95 mg/kg
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111 to 125 kg
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115 mg
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1.04 to 0.92 mg/kg
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126 to 136 kg
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135 mg
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1.07 to 0.99 mg/kg
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aER = extended release.
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Approval:
Six months (maximum effect may take upwards of 3-6 months)
Last review date: July 25, 2016