|
| U.S. Brand
Names |
|
| Panhematin® |

|
|
| Generic
Available |
|
|
No |

|
|
| Pharmacological Index |
|
|
Blood Modifiers |

|
|
| Use |
|
|
Treatment of recurrent attacks of acute intermittent porphyria (AIP) only
after an appropriate period of alternate therapy has been
tried |

|
|
| Contraindications |
|
|
Porphyria cutanea tarda; hypersensitivity to hemin |

|
|
| Adverse
Reactions |
|
|
1% to 10%:
Hematologic: Leukocytosis
Local: Phlebitis |

|
|
| Drug
Interactions |
|
|
Estrogens, barbiturates, corticosteroids, anticoagulants |

|
|
| Usual Dosage |
|
|
I.V.: 1-4 mg/kg/day administered over 10-15 minutes for 3-14 days; may be
repeated no earlier than every 12 hours; not to exceed 6 mg/kg in any 24-hour
period |

|
|
| Mental Health: Effects
on Mental Status |
|
|
None reported |

|
|
| Mental Health:
Effects on Psychiatric
Treatment |
|
|
Avoid concurrent use with barbiturates |

|
|
| Dental Health: Local
Anesthetic/Vasoconstrictor
Precautions |
|
|
No information available to require special precautions |

|
|
| Dental Health:
Effects on Dental Treatment |
|
|
No effects or complications reported |

|
|
| Dosage Forms |
|
|
Powder for injection, preservative free: 313 mg/vial [hematin 7 mg/mL] (43
mL) |

|
|
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|