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Zyprexa (olanzapine, olanzapine) 10 mg, is supplied as blue.

Zyprexa pde5 inhibitors such as relax smooth muscle and increase blood flow to the penis. May be taken with or without food.

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Olanzapine
Clinical data
Trade namesZyprexa, others [1]
AHFS/Drugs.comMonograph
MedlinePlusa601213
License dataEU  EMA:  by INN, US   FDA: Olanzapine
Pregnancy categoryAU: C US: C (Risk not ruled out)
Routes of administrationBy mouth, intramuscular injection
ATC codeN05AH03 ( WHO )
Legal status
Legal statusAU: S4 (Prescription only) CA : ℞-only NZ : Prescription medicine, UK: POM (Prescription only) US: ℞-only
Pharmacokinetic data
Bioavailability87% [2]
Protein binding93% [3]
MetabolismHepatic (direct glucuronidation and CYP1A2 mediated oxidation)
Elimination half-life33 hours, 51.8 hours (elderly) [3]
ExcretionUrine (57%; 7% as unchanged drug), faeces (30%) [3] [4]

Generic Zyprexa Zydis Availability

History of seizures. Bipolar disorder:

Two or more reference listed drugs are generally selected only when there are at least two potential reference drug products which are not bioequivalent to each other. Dissolve in mouth and swallow with or without fluids.

AB Products meeting necessary bioequivalence requirements.

Two or more reference listed drugs are generally selected only when there are at least two potential reference drug products which are not bioequivalent to each other. Discontinue if neuroleptic malignant syndrome occurs or if DRESS is suspected; consider discontinuation if tardive dyskinesia occurs.

Boxed Warning:

zyprexa other names:
  1. olanzapina 20 mg
  2. olanzapine pamoate 10 mg
  3. ozace 7 mg
  4. zydis 5 mg

AB Products meeting necessary bioequivalence requirements. In certain instances, a number is added to the end of the AB code source webpage make a three character code i. Monitor for hyperglycemia, hyperlipidemia; do fasting zyprexa zydis generic glucose and lipids testing at beginning, and during therapy.

Increased mortality in elderly patients with dementia-related psychosis. Concomitant lithium or valproate:

Zyprexa information
Drug name zyprexa
Zyprexa alternative name olanzapine pamoate, olanzapinum, olanzepine, ozace
Active substance olanzapine, olanzapine
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Prostatic hypertrophy. Bipolar disorder: Mood disorders: Perform fall risk assessments when initiating and recurrently on long-term therapy.

For both: Patent and Trademark Office and assigns exclusive legal right to the patent holder to protect the proprietary chemical formulation. Conditions that affect metabolism or hemodynamic responses.

Exclusivity periods can run from days to seven years depending upon the circumstance of the exclusivity grant. History of seizures. Prostatic hypertrophy.

Exclusivity periods can run from days to seven years depending upon the circumstance of the exclusivity grant. Suicidal ideation monitor.

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Psychosis:

If a study is submitted that demonstrates bioequivalence to a specific listed drug product, the generic product will be given the same three-character code as the reference listed drug it was compared against.

Mood disorders: - zyprexa (olanzapine).

By designating a single reference listed drug as the standard to which all generic versions must be shown to be bioequivalent, FDA hopes to avoid possible significant variations among generic drugs and their brand name counterpart. Combination therapies: Drug Exclusivity Exclusivity is the sole marketing rights granted by the FDA to a manufacturer upon the zyprexa zydis generic of a drug and may run simultaneously with a patent.

Discontinue if neuroleptic malignant syndrome occurs or if DRESS is suspected; consider discontinuation if tardive dyskinesia occurs.

Pregnancy Cat. In combination with fluoxetine: History of seizures.

AB Products meeting necessary bioequivalence requirements. Bipolar depression: Elderly with dementia-related psychosis not approved use ; increased risk of death or cerebrovascular events eg, stroke, TIA.

  • Pregnancy Cat
  • Increased mortality in elderly patients with dementia-related psychosis
  • Perform fall risk assessments when initiating and recurrently on long-term therapy
  • Narrow angle glaucoma
  • Suicidal ideation monitor

Zyprexa zydis generic

Increased mortality in elderly patients with dementia-related psychosis. If a study is submitted that demonstrates bioequivalence to a specific listed drug product, the revia high product will be given the same three-character code as the reference listed drug it was compared against. History of seizures.

Risk of hypotension, hepatic impairment, slow metabolizers, or sensitive to olanzapine: Conditions that affect metabolism or hemodynamic responses.

Dose adjustments:

Bipolar depression: Elderly with dementia-related psychosis not approved use ; increased risk of death or cerebrovascular events eg, stroke, TIA.

Monitor for weight gain. Mood disorders: Narrow angle glaucoma. Two or more reference listed drugs are generally selected only when there are at least two potential reference drug products which are not bioequivalent to each other.

Nursing mothers Cardio- or cerebrovascular disease Cardio- or cerebrovascular disease Multisource drug products listed under the same heading i
Increased mortality in elderly patients with dementia-related psychosis Cardio- or cerebrovascular disease Monitor for weight gain Suicidal ideation monitor
Three-character codes are assigned only in situations when more than one reference listed drug of the same strength has been designated under the same heading Cardio- or cerebrovascular disease Nursing mothers History of paralytic ileus or breast cancer
Risk of hypotension Cardio- or cerebrovascular disease By designating a single reference listed drug as the standard to which all generic versions must be shown to be bioequivalent Patent and Trademark Office and assigns exclusive legal right to the patent holder to protect the proprietary chemical formulation
In certain instances Monitor for weight gain Exposure to extreme heat Cardio- or cerebrovascular disease
Increased mortality in elderly patients with dementia-related psychosis Narrow angle glaucoma Exposure to extreme heat Prostatic hypertrophy

Risk of hypotension, hepatic impairment, slow metabolizers, or sensitive to olanzapine: Multisource drug products listed under the same heading i. Drug Exclusivity Exclusivity is the sole marketing rights granted by the FDA to a manufacturer upon the approval of a drug and may run simultaneously with a patent.

Dose adjustments: Elderly with dementia-related psychosis not approved use ; increased risk of death or cerebrovascular events eg, stroke, TIA.

Narrow angle glaucoma. Monitor for weight gain. AB Products meeting necessary bioequivalence requirements. Exclusivity periods can run from days to seven years depending upon the circumstance of the exclusivity grant and blog here.

See Also: Reevaluate periodically.

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Concomitant lithium or valproate: For both:


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