Gravitate Health FHIR Implementation Guide
0.1.0 - CI Build

Ingredient

Role: inactive ingredient

Substance: FERRIC OXIDE RED

Ingredient

Role: inactive ingredient

Substance: HYPROMELLOSE 2910 (6 MPA.S)

Ingredient

Role: inactive ingredient

Substance: MAGNESIUM STEARATE

Ingredient

Role: inactive ingredient

Substance: MICROCRYSTALLINE CELLULOSE

Ingredient

Role: active ingredient - basis of strength

Substance:

Presentation strength: 75 mg / 1 1

Ingredient

Role: inactive ingredient

Substance: SILICON DIOXIDE

Ingredient

Role: inactive ingredient

Substance: SUCCINIC ACID

Ingredient

Role: inactive ingredient

Substance: 15FIX9V2JP

Ingredient

Role: inactive ingredient

Substance: TRIACETIN

Gravitate Health FHIR Implementation Guide, published by Gravitate Health Project. This guide is not an authorized publication; it is the continuous build for version 0.1.0 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/hl7-eu/gravitate-health/tree/master and changes regularly. See the Directory of published versions
Built from commit 6728682b.

Example Bundle: bundle-ibrance75-100-125

Composition category:
Composition status: final
Composition type: HUMAN PRESCRIPTION LABEL

SPL PATIENT PACKAGE INSERT SECTION

PATIENT INFORMATION

IBRANCE ® (EYE-brans)
(palbociclib)

Tablets

What is the most important information I should know about IBRANCE?

IBRANCE may cause serious side effects, including:

Low white blood cell counts (neutropenia). Low white blood cell counts are very common when taking IBRANCE and may cause serious infections that can lead to death. Your healthcare provider should check your white blood cell counts before and during treatment.

If you develop low white blood cell counts during treatment with IBRANCE, your healthcare provider may stop your treatment, decrease your dose, or may tell you to wait to begin your treatment cycle. Tell your healthcare provider right away if you have signs and symptoms of low white blood cell counts or infections such as fever and chills.

Lung problems (pneumonitis). IBRANCE may cause severe or life-threatening inflammation of the lungs during treatment that can lead to death. Tell your healthcare provider right away if you have any new or worsening symptoms, including:

Your healthcare provider may interrupt or stop treatment with IBRANCE completely if your symptoms are severe.

See "What are the possible side effects of IBRANCE?" for more information about side effects.

What is IBRANCE?

IBRANCE is a prescription medicine used in adults to treat hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative breast cancer that has spread to other parts of the body (metastatic) in combination with:

It is not known if IBRANCE is safe and effective in children.

Before taking IBRANCE, tell your healthcare provider about all of your medical conditions, including if you:

Tell your healthcare provider about all of the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements. IBRANCE and other medicines may affect each other causing side effects.

How should I take IBRANCE?

What are the possible side effects of IBRANCE?

IBRANCE may cause serious side effects. See "What is the most important information I should know about IBRANCE?"

The most common side effects of IBRANCE when used with either letrozole or fulvestrant include:

IBRANCE may cause fertility problems in males. This may affect your ability to father a child. Talk to your healthcare provider about family planning options before starting IBRANCE if this is a concern for you.

These are not all of the possible side effects of IBRANCE.

Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.

How should I store IBRANCE?

Keep IBRANCE and all medicines out of the reach of children.

General information about the safe and effective use of IBRANCE

Medicines are sometimes prescribed for purposes other than those listed in a Patient Information leaflet. Do not use IBRANCE for a condition for which it was not prescribed. Do not give IBRANCE to other people, even if they have the same symptoms you have. It may harm them. You can ask your pharmacist or healthcare provider for more information about IBRANCE that is written for health professionals.

What are the ingredients in IBRANCE?

Active ingredient: palbociclib

Inactive ingredients: microcrystalline cellulose, colloidal silicon dioxide, crospovidone, magnesium stearate, succinic acid, HPMC 2910/hypromellose, titanium dioxide, triacetin, and FD&C Blue #2/Indigo Carmine Aluminum Lake. In addition, the 75 mg and 125 mg tablets contain red iron oxide and the 100 mg tablets contain yellow iron oxide.

Pfizer Logo

LAB-1372-1.0

For more information, go to www.IBRANCE.com or call 1-800-438-1985.

PRINCIPAL DISPLAY PANEL - TOPPER CARD

Your Monthly Box

Includes 3 weekly packs of 

IBRANCE® (palbociclib) medication.

Fill in the dates below to help track your treatment cycle.

Treatment Cycle

Week 1   Week 2   Week 3

IBRANCE

Week 4

No IBRANCE

My Treatment Cycle Tracker

I start my Week 1 

treatment cycle on: 

________ / ______

MONTH     DAY

After Week 4, I will start my

next treatment cycle on:

________ / ______

MONTH     DAY

PAA119239

TOPPER CARD

PRINCIPAL DISPLAY PANEL - 75 MG TABLET DOSE PACK

Pfizer

NDC 0069-0284-07

IBRANCE® 

(palbociclib)

tablets

75 mg per tablet

This weekly pack contains:

7 tablets

Rx only

75 MG TABLET DOSE PACK

PRINCIPAL DISPLAY PANEL - 75 MG TABLET DOSE PACK CARTON

Pfizer

NDC 0069-0284-03

IBRANCE® 

(palbociclib)

tablets

75 mg

21 tablets

Monthly Box Contains: 3 individual weekly

packs. Each pack contains 7 IBRANCE tablets

(75 mg per tablet).

Rx only

Safety

Label

75 MG TABLET DOSE PACK CARTON

PRINCIPAL DISPLAY PANEL - 100 MG TABLET DOSE PACK

Pfizer

NDC 0069-0486-07

IBRANCE® 

(palbociclib)

tablets

100 mg per tablet

This weekly pack contains:

7 tablets

Rx only

100 MG TABLET DOSE PACK

PRINCIPAL DISPLAY PANEL - 100 MG TABLET DOSE PACK CARTON

Pfizer

NDC 0069-0486-03

IBRANCE® 

(palbociclib)

tablets

100 mg

21 tablets

Monthly Box Contains: 3 individual weekly

packs. Each pack contains 7 IBRANCE tablets

(100 mg per tablet).

Rx only

Safety

Label

100 MG TABLET DOSE PACK CARTON

PRINCIPAL DISPLAY PANEL - 125 MG TABLET DOSE PACK

Pfizer

NDC 0069-0688-07

IBRANCE® 

(palbociclib)

tablets

125 mg per tablet

This weekly pack contains:

7 tablets

Rx only

125 MG TABLET DOSE PACK

PRINCIPAL DISPLAY PANEL - 125 MG TABLET DOSE PACK CARTON

Pfizer

NDC 0069-0688-03

IBRANCE® 

(palbociclib)

tablets

125 mg

21 tablets

Monthly Box Contains: 3 individual weekly

packs. Each pack contains 7 IBRANCE tablets

(125 mg per tablet).

Rx only

Safety

Label

125 MG TABLET DOSE PACK CARTON

IBRANCE® (palbociclib) tablets - 75 mg

NDC: 0069-0284

Full name: IBRANCE® (palbociclib) tablets - 75 mg

Name usage: English (United States of America)


Authorised dose form: Film Coated Tablet Dosage Form

Legal status of supply: Marketing Authorization

Domain: Human

Resource status: Active


Product classification:

Marketing Authorization 1 of 4

Authorisation number: 0069-0284-03

Region: United States of America

Marketing authorisation holder: Pfizer Laboratories Div Pfizer Inc

Identifier:

Status: Approved for Human Use Product (2020-03-30T00:00:00Z)

Package: 1 Carton

Containing: 3

Manufactured Item

Dose form: Film Coated Tablet Dosage Form

Unit of presentation: Tablet Dosing Unit

Ingredient

Role: inactive ingredient

Substance: CROSPOVIDONE

Ingredient

Role: inactive ingredient

Substance: FD&C BLUE NO. 2 /b>

Package 1 of 6

NDC: NDC:0069-0284-03

Description: 3 in 1 CARTON

Marketing status:

Pack size:
  • 1
  • Package: 1 Dose Pack

    Containing: 7

    Manufactured Item

    Dose form: Film Coated Tablet Dosage Form

    Unit of presentation: Tablet Dosing Unit

    Ingredient

    Role: inactive ingredient

    Substance: CROSPOVIDONE

    Ingredient

    Role: inactive ingredient

    Substance: FD&C BLUE NO. 2 /b>

    Package 2 of 6

    NDC: NDC 0069-0284-07

    7 in 1 DOSE PACK; Type 0: Not a Combination Product

    Description:

    Marketing status:

    Pack size:
  • 1
  • Ingredient

    Role: inactive ingredient

    Substance: FERRIC OXIDE RED

    Ingredient

    Role: inactive ingredient

    Substance: HYPROMELLOSE 2910 (6 MPA.S)

    Ingredient

    Role: inactive ingredient

    Substance: MAGNESIUM STEARATE

    Ingredient

    Role: inactive ingredient

    Substance: MICROCRYSTALLINE CELLULOSE

    Ingredient

    Role: active ingredient - basis of strength

    Substance:

    Presentation strength: 75 mg / 1 1

    Ingredient

    Role: inactive ingredient

    Substance: SILICON DIOXIDE

    Ingredient

    Role: inactive ingredient

    Substance: SUCCINIC ACID

    Ingredient

    Role: inactive ingredient

    Substance: 15FIX9V2JP

    Ingredient

    Role: inactive ingredient

    Substance: TRIACETIN

    Administrable Product (1 of 3)

    Dose form: Film Coated Tablet Dosage Form

    Unit of presentation: Tablet Dosing Unit

    Route of administration:

    Ingredients: