Parkesteron

Parkesteron may be available in the countries listed below.

In some countries, this medicine may only be approved for veterinary use.

Ingredient matches for Parkesteron

Neomycin

Neomycin sulfate (a derivative of Neomycin) is reported as an ingredient of Parkesteron in the following countries:

• Germany

Nystatin

Nystatin is reported as an ingredient of Parkesteron in the following countries:

• Germany

Thiostrepton

Thiostrepton is reported as an ingredient of Parkesteron in the following countries:

• Germany

Triamcinolone

Triamcinolone 16α,17α-acetonide (a derivative of Triamcinolone) is reported as an ingredient of Parkesteron in the following countries:

• Germany

International Drug Name Search

Acetaminophen/Caffeine/Phenyltoloxamine

Pronunciation: ah-seet-ah-MIN-oh-fen/ka-FEEN/fen-ill-tole-OX-a-meen
Generic Name: Acetaminophen/Caffeine/Phenyltoloxamine
Brand Name: Flextra

Acetaminophen/Caffeine/Phenyltoloxamine is used for:

Treating mild to moderate aches and pains associated with headache, muscle and joint soreness, backache, menstrual cramps, colds and flu, sinusitis, toothache, and minor pain from arthritis. It may also be used for other conditions as determined by your doctor.

Acetaminophen/Caffeine/Phenyltoloxamine is an analgesic, antihistamine, and antipyretic combination. It works by blocking substances in the body that cause fever, pain, and inflammation. It also blocks histamine, which causes sneezing and itchy, watery eyes.

Do NOT use Acetaminophen/Caffeine/Phenyltoloxamine if:

• you are allergic to any ingredient in Acetaminophen/Caffeine/Phenyltoloxamine


• you have lung problems (eg, asthma, emphysema, chronic obstructive pulmonary disease [COPD]), difficulty urinating due to an enlarged prostate, glaucoma, or blood clotting problems


• you are taking medicine for blood clotting or sodium oxybate (GHB)

Contact your doctor or health care provider right away if any of these apply to you.

Before using Acetaminophen/Caffeine/Phenyltoloxamine:

Some medical conditions may interact with Acetaminophen/Caffeine/Phenyltoloxamine. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

• if you are pregnant, planning to become pregnant, or are breast-feeding


• if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement


• if you have allergies to medicines, foods, or other substances


• if you have bleeding problems, blood vessel problems in the brain, blockage of the stomach or bowel, kidney or liver problems, chickenpox, flu, rheumatoid arthritis, Kawasaki syndrome, prostate problems, blockage of the bladder, or difficulty urinating

Some MEDICINES MAY INTERACT with Acetaminophen/Caffeine/Phenyltoloxamine. Tell your health care provider if you are taking any other medicines, especially any of the following:

• Isoniazid, sodium oxybate (GHB), sympathomimetics (eg, pseudoephedrine), or theophyllines (eg, aminophylline) because the risk of side effects may be increased


• Blood thinners (eg, warfarin) because the risk of side effects, including the risk of bruising or bleeding, may be increased


• Barbiturates (eg, phenobarbital) because the effectiveness of Acetaminophen/Caffeine/Phenyltoloxamine may be decreased

This may not be a complete list of all interactions that may occur. Ask your health care provider if Acetaminophen/Caffeine/Phenyltoloxamine may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How to use Acetaminophen/Caffeine/Phenyltoloxamine:

Use Acetaminophen/Caffeine/Phenyltoloxamine as directed by your doctor. Check the label on the medicine for exact dosing instructions.

• Acetaminophen/Caffeine/Phenyltoloxamine may be taken with or without food.


• If you miss a dose of Acetaminophen/Caffeine/Phenyltoloxamine and you are using it regularly, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about how to use Acetaminophen/Caffeine/Phenyltoloxamine.

Important safety information:

• Acetaminophen/Caffeine/Phenyltoloxamine may cause drowsiness. Do not drive, operate machinery, or do anything else that could be dangerous until you know how you react to Acetaminophen/Caffeine/Phenyltoloxamine. Using Acetaminophen/Caffeine/Phenyltoloxamine alone, with certain other medicines, or with alcohol may lessen your ability to drive or perform other potentially dangerous tasks.


• Avoid drinking alcohol or taking other medications that cause drowsiness (eg, sedatives, tranquilizers) while taking Acetaminophen/Caffeine/Phenyltoloxamine. Acetaminophen/Caffeine/Phenyltoloxamine will add to the effects of alcohol and other depressants. Ask your pharmacist if you have questions about which medicines are depressants.


• Acetaminophen/Caffeine/Phenyltoloxamine may cause liver damage. If you consume 3 or more alcohol-containing drinks every day, ask your doctor if you should take Acetaminophen/Caffeine/Phenyltoloxamine or other pain relievers/fever reducers. Alcohol use combined with Acetaminophen/Caffeine/Phenyltoloxamine may increase your risk for liver damage.


• Acetaminophen/Caffeine/Phenyltoloxamine contains acetaminophen. Before you begin taking any new prescription or nonprescription medicine, read the ingredients to see if it also contains acetaminophen. If it does or if you are uncertain, contact your doctor or pharmacist.


• Do not exceed the recommended dosage or take Acetaminophen/Caffeine/Phenyltoloxamine for longer than prescribed without checking with your doctor.


• Avoid large amounts of caffeine-containing foods and beverages, such as coffee, tea, cocoa, cola drinks, and chocolate.


• If you are taking Acetaminophen/Caffeine/Phenyltoloxamine for pain or fever and your symptoms do not improve within 10 days or if they become worse, check with your doctor.


• Before you have any medical or dental treatments, emergency care, or surgery, tell the doctor or dentist that you are using Acetaminophen/Caffeine/Phenyltoloxamine.


• Acetaminophen/Caffeine/Phenyltoloxamine is not recommended for use in CHILDREN younger than 12 years of age. Safety and effectiveness in this age group have not been established.


• PREGNANCY and BREAST-FEEDING: If you become pregnant, discuss with your doctor the benefits and risks of using Acetaminophen/Caffeine/Phenyltoloxamine during pregnancy. Acetaminophen/Caffeine/Phenyltoloxamine is excreted in breast milk. Do not breast-feed while taking Acetaminophen/Caffeine/Phenyltoloxamine.

Possible side effects of Acetaminophen/Caffeine/Phenyltoloxamine:

All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:

Anxiety; drowsiness; dry mouth, nose, or throat; heartburn; nausea; nervousness; thickening of mucus in the nose and throat; upset stomach.

Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); bloody or black stools; confusion; dark urine or pale stools; decreased urination; diarrhea; difficulty swallowing; dizziness; hearing loss; hoarseness; persistent sore throat or other signs of infection; ringing in the ears; severe stomach pain; unusual bruising or bleeding; unusual tiredness; vomiting; yellowing of the skin or eyes.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.

See also: Acetaminophen/Caffeine/Phenyltoloxamine side effects (in more detail)

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately. Symptoms may include abnormal behavior; dark urine; excessive sweating; extreme tiredness; fast or deep breathing; loss of consciousness; ringing in the ears; stomach pain; vomiting.

Proper storage of Acetaminophen/Caffeine/Phenyltoloxamine:

Store at room temperature, 77 degrees F (25 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Acetaminophen/Caffeine/Phenyltoloxamine out of the reach of children and away from pets.

General information:

• If you have any questions about Acetaminophen/Caffeine/Phenyltoloxamine, please talk with your doctor, pharmacist, or other health care provider.


• Acetaminophen/Caffeine/Phenyltoloxamine is to be used only by the patient for whom it is prescribed. Do not share it with other people.


• If your symptoms do not improve or if they become worse, check with your doctor.


• Check with your pharmacist about how to dispose of unused medicine.

This information is a summary only. It does not contain all information about Acetaminophen/Caffeine/Phenyltoloxamine. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.

Issue Date: February 1, 2012

Database Edition 12.1.1.002

Copyright © 2012 Wolters Kluwer Health, Inc.

More Acetaminophen/Caffeine/Phenyltoloxamine resources

• Acetaminophen/Caffeine/Phenyltoloxamine Side Effects (in more detail)
• Acetaminophen/Caffeine/Phenyltoloxamine Use in Pregnancy & Breastfeeding
• Acetaminophen/Caffeine/Phenyltoloxamine Drug Interactions
• Acetaminophen/Caffeine/Phenyltoloxamine Support Group
• 0 Reviews for Acetaminophen/Caffeine/Phenyltoloxamine - Add your own review/rating

Compare Acetaminophen/Caffeine/Phenyltoloxamine with other medications

• Cold Symptoms
• Headache
• Pain
• Sinusitis

Granisetron Stada

Granisetron Stada may be available in the countries listed below.

Ingredient matches for Granisetron Stada

Granisetron

Granisetron hydrochloride (a derivative of Granisetron) is reported as an ingredient of Granisetron Stada in the following countries:

• Austria


• Germany

International Drug Name Search

Carbon Dioxide Oxygen Mixture

Dosage Form: gas
Carbon Dioxide Oxygen Mixture

COMPRESSED GAS, OXIDIZING, N.O.S.

(  % CARBON DIOXIDE USP,    %OXYGEN USP) UN 3156 NON-FLAMMABLE 2    OXIDIZER 5.1   30460D (06/02)

OXYGEN CONTENT OVER 23.5% Rx only. CAUTION: FEDERAL LAW PROHIBITS DISPENSING WITHOUT A PRESCRIPTION. WARNING: Administration of this gas may be hazardous or contraindicated. For use only by under the supervision of a licensed practitioner who is experienced in the use and administration of gas mixtures and is familiar with the indications, effects, dosages, methods, and frequency and duration of administration, and with the hazards, contraindication and side effects, and the precautions to be taken. CAUTION: HIGH PRESSURE OXIDIZING GAS. VIGOROUSLY ACCELERATES COMBUSTION. MIXTURES CONTAINING CARBON DIOXIDE CAN INCREASE RESPIRATION AND HEART RATE. Keep oil and grease away. Open valve slowly. Store and use with adequate ventilation. Use only with equipment cleaned for oxygen service and rated for cylinder pressure. Cylinder temperature should not exceed 52C (125F). Close valve after each use and when empty. Use in accordance with the Material Safety Data Sheet (MSDS). FIRST AID: IF INHALED, remove to fresh air. If not breathing, give artificial respiration. If breathing is difficult, give oxygen. Call a physician.  CARBON DIOXIDE CAS: 124-38-9 OXYGEN CAS: 7782-44-7 DO NOT REMOVE THIS PRODUCT LABEL.

FILLED and INSPECTED BY GENERAL AIR SERVICE and SUPPLY DENVER, CO 80204

COMPRESSED GAS, OXIDIZING, N.O.S.

(  % CARBON DIOXIDE USP,    %OXYGEN USP) UN 3156 NON-FLAMMABLE 2    OXIDIZER 5.1   30460D (06/02)

OXYGEN CONTENT OVER 23.5% Rx only. CAUTION: FEDERAL LAW PROHIBITS DISPENSING WITHOUT A PRESCRIPTION. WARNING: Administration of this gas may be hazardous or contraindicated. For use only by under the supervision of a licensed practitioner who is experienced in the use and administration of gas mixtures and is familiar with the indications, effects, dosages, methods, and frequency and duration of administration, and with the hazards, contraindication and side effects, and the precautions to be taken. CAUTION: HIGH PRESSURE OXIDIZING GAS. VIGOROUSLY ACCELERATES COMBUSTION. MIXTURES CONTAINING CARBON DIOXIDE CAN INCREASE RESPIRATION AND HEART RATE. Keep oil and grease away. Open valve slowly. Store and use with adequate ventilation. Use only with equipment cleaned for oxygen service and rated for cylinder pressure. Cylinder temperature should not exceed 52C (125F). Close valve after each use and when empty. Use in accordance with the Material Safety Data Sheet (MSDS). FIRST AID: IF INHALED, remove to fresh air. If not breathing, give artificial respiration. If breathing is difficult, give oxygen. Call a physician.  CARBON DIOXIDE CAS: 124-38-9 OXYGEN CAS: 7782-44-7 DO NOT REMOVE THIS PRODUCT LABEL.

FILLED and INSPECTED BY GENERAL AIR SERVICE and SUPPLY DENVER, CO 80204

Carbon Dioxide Oxygen Mixture  Carbon Dioxide Oxygen Mixture  gas

Product Information Product Type HUMAN PRESCRIPTION DRUG NDC Product Code (Source) 21220-129 Route of Administration RESPIRATORY (INHALATION) DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Carbon Dioxide (Carbon Dioxide) Carbon Dioxide 200 mL  in 1 L Oxygen (Oxygen) Oxygen 800 mL  in 1 L

Inactive Ingredients Ingredient Name Strength No Inactive Ingredients Found

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 21220-129-01 7101 L In 1 CYLINDER None 2 21220-129-02 707 L In 1 CYLINDER None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved medical gas		01/01/1975

Labeler - General Air Service & Supply Co (151227338)

Establishment
Name	Address	ID/FEI	Operations
General Air Service & Supply Co		006686091	manufacture

Revised: 10/2010General Air Service & Supply Co

Vertizon

Vertizon may be available in the countries listed below.

Ingredient matches for Vertizon

Cinnarizine

Cinnarizine is reported as an ingredient of Vertizon in the following countries:

• Vietnam

International Drug Name Search

Erbitux

Pronunciation: se-TUX-i-mab
Generic Name: Cetuximab
Brand Name: Erbitux

Serious and sometimes fatal reactions have occurred in patients receiving Erbitux. Many of the reactions have occurred during the first dose. If you develop symptoms such as sudden trouble breathing; hoarseness; wheezing; hives; itching; fever; chills; severe dizziness; fainting; swelling of the mouth, face, lips, or tongue; chest pain or tightness; or numbness of an arm or leg, seek immediate medical attention.

The risk of heart attack or sudden death may be increased in patients who receive Erbitux along with radiation to treat certain types of cancer of the head and neck. Be sure to tell your doctor if you have heart blood vessel problems, heart failure, or an irregular heartbeat. Lab tests, including blood electrolytes, may be performed while you use Erbitux and for a period of time after you finish Erbitux.

Erbitux is used for:

Treating certain types of head, neck, and colorectal cancer. Erbitux may be used alone or along with radiation treatments or other medicines. It may also be used for other conditions as determined by your doctor.

Erbitux is a monoclonal antibody. It works by blocking a certain growth factor. This helps to reduce the growth and survival of certain types of cancer cells.

Do NOT use Erbitux if:

• you are allergic to any ingredient in Erbitux

Contact your doctor or health care provider right away if any of these apply to you.

Before using Erbitux:

Some medical conditions may interact with Erbitux. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

• if you are pregnant, planning to become pregnant, or are breast-feeding


• if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement


• if you have allergies to medicines, foods, or other substances (eg, mouse proteins)


• if you have lung problems (eg, interstitial lung disease, pulmonary fibrosis), abnormal blood electrolyte levels, breathing problems, or a respiratory tract infection


• if you have a history of blood vessel problems, heart problems, heart failure, or irregular heartbeat


• if you are having radiation therapy or other types of chemotherapy (eg, cisplatin)

Some MEDICINES MAY INTERACT with Erbitux. However, no specific interactions with Erbitux are known at this time.

Ask your health care provider if Erbitux may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How to use Erbitux:

Use Erbitux as directed by your doctor. Check the label on the medicine for exact dosing instructions.

• Erbitux is usually given as an injection at your doctor's office, hospital, or clinic. If you will be using Erbitux at home, a health care provider will teach you how to use it. Be sure you understand how to use Erbitux. Follow the procedures you are taught when you use a dose. Contact your health care provider if you have any questions.


• Do not use Erbitux if it contains particles, is cloudy or discolored, or if the vial is cracked or damaged.


• Do not shake or dilute Erbitux.


• Keep this product, as well as syringes and needles, out of the reach of children and pets. Do not reuse needles, syringes, or other materials. Ask your health care provider how to dispose of these materials after use. Follow all local rules for disposal.


• If you miss a dose of Erbitux, contact your doctor right away.

Ask your health care provider any questions you may have about how to use Erbitux.

Important safety information:

• Erbitux may cause dizziness. This effect may be worse if you take it with alcohol or certain medicines. Use Erbitux with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it.


• Erbitux may cause you to become sunburned more easily. Avoid the sun, sunlamps, or tanning booths until you know how you react to Erbitux. If you must be outside for more than a short time, use a sunscreen or wear protective clothing while you use Erbitux and for 2 months after your last dose.


• If nausea, loss of appetite, vomiting, or diarrhea occurs, you will need to take care not to become dehydrated. Contact your doctor for instructions on how to lessen these effects.


• Erbitux may lower the ability of your body to fight infection. Avoid contact with people who have colds or infections. Tell your doctor if you notice signs of infection like fever, sore throat, rash, or chills.


• Men who take Erbitux should always use a condom when having sex with a woman who may become pregnant. Do this for as long as you take Erbitux and for 6 months after you stop taking it.


• Women who are able to become pregnant should use effective birth control while using Erbitux and for at least 6 months after the last dose.


• Lab tests, including blood electrolytes, may be performed while you use Erbitux and for 8 weeks after you stop using it. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.


• Erbitux should be used with extreme caution in CHILDREN; safety and effectiveness in children have not been confirmed.


• PREGNANCY and BREAST-FEEDING: It is not known if Erbitux can cause harm to the fetus. If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Erbitux while you are pregnant. It is not known if Erbitux is found in breast milk. Do not breast-feed while using Erbitux or for 2 months after you stop taking it.

Possible side effects of Erbitux:

All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:

Changes in fingernails or toenails; constipation; cough; diarrhea; dry mouth; dry skin; eye redness or irritation; general body discomfort; headache; indigestion; mild acne; nausea; pain, swelling, or redness at the injection site; sore throat; stomach pain or upset; tiredness; trouble sleeping; vomiting; weakness; weight loss.

Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); breathing problems or shortness of breath; change in the amount of urine produced; chest pain; confusion; eye or eyelid redness, swelling, or irritation; fainting; fever, chills, or persistent sore throat; hoarseness; increased abnormal hair growth; mental or mood changes (eg, anxiety, depression); numbness of an arm or leg; peeling, redness, cracking, or oozing of the skin; severe or persistent acne; severe or persistent dizziness or headache; severe or persistent stomach pain, nausea, or vomiting; severe or persistent tiredness or weakness; sores on the lips or in the mouth; swelling of the hands, legs, or feet; trouble swallowing; vision changes; wheezing.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.

See also: Erbitux side effects (in more detail)

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately.

Proper storage of Erbitux:

Erbitux is usually handled and stored by a health care provider. If you are using Erbitux at home, store Erbitux as directed by your pharmacist or health care provider.

General information:

• If you have any questions about Erbitux, please talk with your doctor, pharmacist, or other health care provider.


• Erbitux is to be used only by the patient for whom it is prescribed. Do not share it with other people.


• If your symptoms do not improve or if they become worse, check with your doctor.


• Check with your pharmacist about how to dispose of unused medicine.

This information is a summary only. It does not contain all information about Erbitux. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.

Issue Date: February 1, 2012

Database Edition 12.1.1.002

Copyright © 2012 Wolters Kluwer Health, Inc.

More Erbitux resources

• Erbitux Side Effects (in more detail)
• Erbitux Use in Pregnancy & Breastfeeding
• Erbitux Drug Interactions
• Erbitux Support Group
• 2 Reviews for Erbitux - Add your own review/rating

• Erbitux Prescribing Information (FDA)


• Erbitux Consumer Overview


• Erbitux Monograph (AHFS DI)


• Erbitux Advanced Consumer (Micromedex) - Includes Dosage Information


• Cetuximab Professional Patient Advice (Wolters Kluwer)

Compare Erbitux with other medications

• Colorectal Cancer
• Head and Neck Cancer
• Squamous Cell Carcinoma

Lisi-Hennig

Lisi-Hennig may be available in the countries listed below.

Ingredient matches for Lisi-Hennig

Lisinopril

Lisinopril dihydrate (a derivative of Lisinopril) is reported as an ingredient of Lisi-Hennig in the following countries:

• Germany

International Drug Name Search