Tamiflu 45 mg hard capsules

Spain
Brand name Tamiflu 45 mg hard capsules
Form capsules, hard
Active substance / Dosage
Prescription type Prescription Only Medicine
Registration number 02222004
Tamiflu 45 mg hard capsules capsules, hard

Package leaflet: Information for the user

Introduction

Package leaflet: information for the user

Tamiflu 45mg hard capsules

oseltamivir

Read all of this leaflet carefully before you start taking this medicine because it contains important information for you.

  • Keep this leaflet. You may need to read it again.
  • If you have any further questions, ask your doctor or pharmacist.
  • This medicine has been prescribed for you only and must not be given to other people, even if they have the same symptoms as you. It could harm them.
  • If you get any side effects, talk to your doctor or pharmacist, even if they are not listed in this leaflet. See section 4.

Contents of the leaflet

  1. What Tamiflu is and what it is used for
  2. What you need to know before you take Tamiflu
  3. How to take Tamiflu
  4. Possible side effects
  5. How to store Tamiflu
  6. Contents of the pack and other information

1. What Tamiflu is and what it is used for

  • Tamiflu is used in adults, adolescents, children, and infants (including full-term newborn babies) for the treatment of influenza (influenza). It may be used when you have symptoms of influenza and it is known that the influenza virus is circulating in the community.
  • Tamiflu may also be prescribed to adults, adolescents, children, and infants over 1 year of age for preventing influenza on a case-by-case basis, for example, if you have been in close contact with someone who has influenza.
  • Tamiflu may be prescribed to adults, adolescents, children, and infants (including full-term newborn babies) as prophylactic treatment under exceptional circumstances, for example, during a global influenza outbreak (an influenza pandemic) and when the seasonal influenza vaccine cannot provide sufficient protection.

Tamiflu contains oseltamivir, which belongs to a group of medicines known as neuraminidase inhibitors. These medicines prevent the spread of the influenza virus within the body. They help to relieve or prevent symptoms caused by influenza virus infection.

Influenza is a viral infection. Signs of influenza often include sudden fever (above 37.8 °C), cough, runny or stuffy nose, headache, muscle aches, and extreme fatigue. These symptoms may also be caused by other infections. A true influenza infection only occurs during annual outbreaks (epidemics), when influenza viruses are circulating in the population. Outside epidemic periods, influenza-like symptoms are generally caused by other types of illness.

2. What you need to know before taking Tamiflu

Do not take Tamiflu

  • if you are allergic (hypersensitive) to oseltamivir or to any of the other ingredients of Tamiflu listed in section 6.

If this applies to you, consult your doctor. Do not take Tamiflu.

Warnings and precautions

Before taking Tamiflu, make sure your doctor knows if:

  • you are allergic to other medicines
  • you have any kidney disease. If so, your dose may need to be adjusted.
  • you have a serious illness requiring immediate hospitalization.
  • your immune system is not working properly.
  • you have chronic heart or respiratory disease.

During treatment with Tamiflu, tell your doctor immediately if:

  • you notice changes in your behaviour or mental state (neuropsychiatric events), especially if they occur in children and adolescents. These may be signs of rare but serious side effects.

Tamiflu is not a flu vaccine

Tamiflu is not a vaccine: it is used to treat infection or prevent the spread of the influenza virus. A vaccine provides antibodies against the virus. Tamiflu does not affect the effectiveness of the flu vaccine, and your doctor may prescribe both.

Use of Tamiflu with other medicines

Tell your doctor or pharmacist if you are taking any other medicines, or have recently taken any, including those obtained without a prescription.

The following medicines are particularly important:

  • chlorpropamide (used to treat diabetes)
  • methotrexate (used to treat, for example, rheumatoid arthritis)
  • phenylbutazone (used to treat pain and inflammation)
  • probenecid (used to treat gout)

Pregnancy and breastfeeding

You must inform your doctor if you are pregnant, think you may be pregnant, or plan to become pregnant, so that your doctor can decide whether Tamiflu is suitable for you.

Effects on infants are unknown. Inform your doctor if you are breastfeeding, so that they can decide whether Tamiflu is suitable for you.

Consult your doctor or pharmacist before using this medicine.

Driving and using machines

Tamiflu has no effect on your ability to drive or operate machinery.

Tamiflu contains sodium:

This medicine contains less than 1 mmol of sodium (23 mg) per capsule; i.e., essentially "sodium-free".

3. How to take Tamiflu

Follow exactly the Tamiflu administration instructions provided by your doctor. Consult your doctor or pharmacist if you have any questions.

Take Tamiflu as soon as possible; ideally, within two days of the onset of flu symptoms.

Recommended doses

For the treatment of influenza, take two doses daily. It is generally advisable to take one dose in the morning and another in the evening. It is important to complete the full 5-day treatment course, even if you start feeling better quickly.

For patients with a weakened immune system, treatment will continue for 10 days.

For the prevention of influenza or after contact with an infected person, take one dose daily for 10 days. It is best to take this dose in the morning with breakfast.

In special situations, such as widespread influenza outbreaks or in patients with a weakened immune system, treatment may continue for up to 6 or 12 weeks.

The recommended dose depends on the patient's body weight. You should use the number of capsules or volume of oral suspension prescribed by your doctor.

Adults and adolescents aged 13 years and older

Body weight

Influenza treatment: dose
for 5 days

Influenza treatment (in immunocompromised patients): dose
for 10 days*

Influenza prevention: dose
for 10 days

Over 40 kg

75 mg** twice daily

75 mg** twice daily

75 mg** once daily

*For patients with a weakened immune system, the treatment duration is 10 days.

**75 mg can be obtained with one 30 mg capsule plus one 45 mg capsule

Children from 1 to 12 years of age

Body weight

Influenza treatment: dose for 5 days

Influenza treatment (in immunocompromised patients): dose for 10 days*

Influenza prevention: dose for 10 days

10 to 15 kg

30 mg twice daily

30 mg twice daily

30 mg once daily

Over 15 kg up to 23 kg

45 mg twice daily

45 mg twice daily

45 mg once daily

Over 23 kg up to 40 kg

60 mg twice daily

60 mg twice daily

60 mg once daily

Over 40 kg

75 mg** twice daily

75 mg** twice daily

75 mg** once daily

*For children with a weakened immune system, the treatment duration is 10 days.

**75 mg can be obtained with one 30 mg capsule plus one 45 mg capsule.

Children under 1 year of age (0 to 12 months)

The administration of Tamiflu to children under 1 year of age for the prevention of influenza during a pandemic should be carried out at the physician's discretion, after considering the potential benefit against any potential risk to the child.

Body weight

Influenza treatment: dose for 5 days

Influenza treatment (in immunocompromised patients): dose for 10 days*

Influenza prevention: dose for 10 days

3 kg to over 10 kg

3 mg per kg body weight**, twice daily

3 mg per kg body weight**, twice daily

3 mg per kg body weight**, once daily

*For children with a weakened immune system, the treatment is 10 days.

**mg per kg = mg per each kilogram of the child's body weight. For example:

If a 6-month-old child weighs 8 kg, the dose is

8 kg x 3 mg per kg = 24 mg

Method of administration

Swallow the capsules whole with water. Do not break or chew the capsules.

Tamiflu may be taken with or without food; however, taking it with food may reduce the likelihood of experiencing discomfort (nausea or vomiting).

People who may have difficulty swallowing the capsules can use a liquid medicine, Tamiflu oral suspension, but if this is not available at your pharmacy, you can prepare a liquid form of Tamiflu from the capsules. See the page onPreparing Tamiflu liquid at home.

If you take more Tamiflu than you should

Stop taking Tamiflu and consult a doctor or pharmacist immediately.

In many cases of overdose, no adverse effects were reported. When adverse effects were reported, they were similar to those seen with normal doses and are included in section 4.

Overdose cases with Tamiflu have been reported more frequently in children than in adults and adolescents. Caution must be exercised when preparing liquid Tamiflu for children and when administering Tamiflu capsules or liquid to children.

If you forget to take Tamiflu

Do not take a double dose to make up for missed doses.

If you stop treatment with Tamiflu

No adverse effects occur when you stop taking Tamiflu. However, if you stop taking Tamiflu before the time prescribed by your doctor, flu symptoms may return. Always complete the course of treatment prescribed by your doctor.

If you have any further questions about the use of this medicine, ask your doctor or pharmacist.

4. Possible adverse effects

Like all medicines, this medicine can cause adverse effects, although not everyone experiences them. Many of these adverse effects may be caused by influenza itself.

Since oseltamivir has been marketed, the following serious adverse effects have rarely been reported:

  • Anaphylactic and anaphylactoid reactions: severe allergic reactions, with facial and skin swelling, itchy rash, low blood pressure, and difficulty breathing.
  • Hepatic disorders (fulminant hepatitis, liver function disorder, and jaundice): yellowing of the skin and whites of the eyes, change in stool color, changes in behavior.
  • Angioneurotic edema: sudden severe swelling of the skin, mainly around the head and neck area, including eyes and tongue, with difficulty breathing.
  • Stevens-Johnson syndrome and toxic epidermal necrolysis: a complicated allergic reaction that may be life-threatening, causing severe inflammation of the outer layer of the skin and possibly internal organs, initially presenting with fever, sore throat, fatigue, skin rash, blistering, peeling, and large areas of skin shedding, possible breathing difficulties, and low blood pressure.
  • Gastrointestinal hemorrhage: prolonged bleeding from the large intestine or vomiting blood.
  • Neuropsychiatric disorders, as described below.

If you notice any of these symptoms, seek medical help immediately.

The most frequently reported adverse effects (very common and common) for Tamiflu are feeling unwell or malaise (nausea, vomiting), stomach pain, stomach discomfort, headache, and pain. These adverse effects usually occur after the first dose of the medicine and generally resolve during the course of treatment. The frequency of these effects is reduced when the medicine is taken with food.

Rare but serious adverse effects: seek medical help immediately

(These may affect up to 1 in 1,000 people)

Rare adverse effects reported during treatment with Tamiflu include:

  • seizures and delirium, including altered levels of consciousness
  • confusion, abnormal behavior
  • delirious disorders, hallucinations, agitation, anxiety, nightmares

These events have been reported mainly in children and adolescents and often began suddenly and resolved quickly. In very rare cases, these events led to self-harm, some with fatal outcomes. These neuropsychiatric events have also been reported in influenza patients who were not taking Tamiflu.

  • Patients, especially children and adolescents, should be closely monitored for the behavioral changes described above.

If you notice any of these symptoms, especially in younger patients, seek medical help immediately.

Adults and adolescents aged 13 years and older

Very common adverse effects

(may affect more than 1 in 10 people)

  • Headache
  • Nausea

Common adverse effects

(may affect up to 1 in 10 people)

  • Bronchitis
  • Chills
  • Cough
  • Dizziness
  • Fever
  • Pain
  • Limb pain
  • Runny nose
  • Difficulty sleeping
  • Sore throat
  • Stomach pain
  • Fatigue
  • Feeling of fullness in the upper abdomen
  • Upper respiratory tract infections (inflammation of nose, throat, and sinuses)
  • Stomach discomfort
  • Vomiting

Uncommon adverse effects

(may affect up to 1 in 100 people)

  • Allergic reactions
  • Altered level of consciousness
  • Seizure
  • Heart rhythm disturbances
  • Mild to severe liver function abnormalities
  • Skin reactions (skin inflammation, red itchy rash, scaly skin)

Rare adverse effects

(may affect up to 1 in 1,000 people)

  • Thrombocytopenia (reduced platelet count)
  • Vision disorders

Children aged 1 to 12 years

Very common adverse effects

(may affect more than 1 in 10 people)

  • Cough
  • Nasal congestion
  • Vomiting

Common adverse effects

(may affect up to 1 in 10 people)

  • Conjunctivitis (red, watery, or painful eyes)
  • Ear inflammation and other ear disorders
  • Headache
  • Nausea
  • Runny nose
  • Stomach pain
  • Feeling of fullness in the upper abdomen
  • Stomach upset

Uncommon adverse effects

(may affect up to 1 in 100 people)

  • Skin inflammation
  • Tympanic membrane disorder (eardrum)

Infants under 1 year of age

Adverse effects reported in children aged 0 to 12 months are mostly similar to those reported in older children (aged 1 year and above). In addition, diarrhea and diaper dermatitis have been reported.

If you consider any of the adverse effects you experience to be severe, or if you notice any adverse effect not mentioned in this leaflet, inform your doctor or pharmacist. However,

  • if you or your child have repeated episodes of illness, or
  • if flu symptoms worsen or fever persists

inform your doctor as soon as possible.

Reporting of adverse effects

If you experience any type of adverse effect, talk to your doctor, even if it is a possible adverse effect not listed in this leaflet. You may also report them directly through the national reporting system listed in Appendix V.

By reporting adverse effects, you can help provide more information on the safety of this medicine.

5. Storage of Tamiflu

Keep this medicine out of the reach and sight of children.

Do not use this medicine after the expiry date which is stated on the packaging and on the blister after EXP. The expiry date refers to the last day of the month indicated.

Do not store above 25 °C.

Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines and packaging you no longer need. This will help protect the environment.

6. Contents of the pack and other information

Composition of Tamiflu

  • The active substance is:

Each hard capsule contains oseltamivir phosphate equivalent to 45 mg of oseltamivir.

  • The other components are:

capsule contents: pregelatinized starch, talc, povidone, sodium croscarmellose,
and sodium stearyl fumarate (see section 2, "Tamiflu contains sodium")

capsule shell: gelatin, black iron oxide (E172), and titanium dioxide (E171)

printing ink: shellac (E904), titanium dioxide (E171), and FD&C Blue No. 2 (indigo
carmine, E132).

Appearance of the product and contents of the pack

The 45 mg hard capsules consist of an opaque grey body marked with "ROCHE" and an opaque grey cap marked with "45 mg". The markings are blue in colour.

Tamiflu 45 mg hard capsules are available in blisters containing 10 capsules.

Marketing Authorization Holder

Roche Registration GmbH
Emil-Barell-Strasse 1
79639 Grenzach-Wyhlen
Germany

Manufacturer responsible for production

Roche Pharma AG
Emil-Barell-Strasse 79639 Grenzach-Wyhlen
Germany

For further information about this medicinal product, please contact the local representative of the Marketing Authorization Holder:

Belgium/Belgium/Belgium

N.V. Roche S.A.

Tel/Tel: +32 (0) 2 525 82 11

Lithuania

UAB “Roche Lietuva”

Tel: +370 5 2546799

Text in Cyrillic characters on a white background stating the name Bulgaria, the phrase Rosh Bulgaria EOOD, and a telephone number with Bulgarian country code

Luxembourg/Luxembourg

(See/siehe Belgium/Belgium)

Czech Republic

Roche s. r. o.

Tel: +420 - 2 20382111

Hungary

Roche (Hungary) Kft.

Tel: +36 - 1 279 4500

Denmark

Roche Pharmaceuticals A/S

Tlf: +45 - 36 39 99 99

Malta

(See Ireland)

Germany

Roche Pharma AG

Tel: +49 (0) 7624 140

Netherlands

Roche Nederland B.V.

Tel: +31 (0) 348 438050

Estonia

Roche Eesti OÜ

Tel: + 372 - 6 177 380

Norway

Roche Norge AS

Tlf: +47 - 22 78 90 00

Greece

Roche (Hellas) A.E.

Tel: +30 210 61 66 100

Austria

Roche Austria GmbH

Tel: +43 (0) 1 27739

Spain

Roche Farma S.A.

Tel: +34 - 91 324 81 00

Poland

Roche Polska Sp.z o.o.

Tel: +48 - 22 345 18 88

France

Roche

Tél: +33 (0) 1 47 61 40 00

Portugal

Roche Farmacêutica Química, Lda

Tel: +351 - 21 425 70 00

Croatia

Roche d.o.o

Tel: +385 1 4722 333

Romania

Roche România S.R.L.

Tel: +40 21 206 47 01

Ireland

Roche Products (Ireland) Ltd.

Tel: +353 (0) 1 469 0700

Slovenia

Roche farmacevtska družba d.o.o.

Tel: +386 - 1 360 26 00

Iceland

Roche Pharmaceuticals A/S

c/o Icepharma hf

Sími: +354 540 8000

Slovakia

Roche Slovensko, s.r.o.

Tel: +421 - 2 52638201

Italy

Roche S.p.A.

Tel: +39 - 039 2471

Finland

Roche Oy

Puh/Tel: +358 (0) 10 554 500

Cyprus

G.A. Stamatīs & Sia Ltd.

Tel: +357 - 22 76 62 76

Sweden

Roche AB

Tel: +46 (0) 8 726 1200

Latvia

Roche Latvija SIA

Tel: +371 - 6 7039831

Date of the most recent review of this leaflet: {MM/YYYY}.

Detailed information on this medicine is available on the European Medicines Agency website: https://www.ema.europa.eu/.


Information for the user

For people who have difficulty swallowing capsules, including very young children, there is a liquid form of this medicine, Tamiflu oral suspension.

If you need a liquid medicine but it is not available, a suspension can be prepared at the pharmacy from Tamiflu capsules (see Information for healthcare professionals). The pharmacy-prepared formulation is the recommended option.

If the pharmacy-prepared formulation is also not available, you may prepare Tamiflu liquid at home from these capsules.

The dose is the same for treatment and for prevention of influenza. The difference is in the frequency of administration.

Preparation of Tamiflu liquid at home

? If you have the correct capsule for the required dose (45 mg dose), open the capsule and mix its contents with a teaspoon (or less) of suitable sweetened food.

This is usually suitable for children over 1 year of age. See the upper section of the instructions.

? If smaller doses are needed, preparing Tamiflu liquid from capsules requires additional steps.

This is suitable for young children, underweight children, and infants: they usually require a Tamiflu dose lower than 45 mg. See the lower section of the instructions.

Children from 1 to 12 years of age

To prepare a 45 mg dose, you will need:

? One 45 mg Tamiflu capsule

? A sharp pair of scissors

? A small container

? Teaspoon (5 ml spoon)

? Water

? Sweetened food to mask the bitter taste of the powder

Examples: chocolate or cherry syrup, dessert sauce, caramel, or condensed milk.

Alternatively, you may prepare sweetened water by mixing one teaspoon of water with three quarters (3/4) of a teaspoon of sugar.

Step 1: Check the correct dose

To determine the correct amount to use, find the patient's weight in the left column of the table.

Look at the right-hand column to check the number of capsules to give the patient for a single dose. The amount is the same for treatment and for prevention of influenza.

dose 45mg

White capsule with the blue text ROCHE on one side and the dosage 45 mg on the other

Only the 45 mg capsules should be used for 45 mg doses. Do not attempt to prepare doses of 30 mg, 60 mg, or 75 mg using the contents of the 45 mg capsules. Instead, use the capsule with the appropriate dose.

Weight

Tamiflu Dose

Number of 45 mg Capsules

Up to 15 kg

30 mg

Do not use 45 mg capsules

Over 15 kg up to 23 kg

45 mg

1 capsule

Over 23 kg up to 40 kg

60 mg

Do not use 45 mg capsules

Step 2: Pour all the powder into the container

Take one 45mg capsule and hold it vertically over a container. Carefully cut off the rounded end with scissors.

Pour all the powder into the container.

Be careful with the powder, as it may be irritating to the skin and eyes.

Black line drawing showing a hand holding a pair of scissors cutting a small object held by another handBlack line drawing of a hand holding tweezers to dip an object into a transparent bowl containing liquid

Step 3: Sweeten the powder and administer the dose

Add a small amount—no more than a teaspoon—of sweetened food to the powder in the container.

This is to mask the bitter taste of Tamiflu powder.

Mix the contents well.

Two hands pouring liquid from a bottle into a spoon held above an empty bowlA hand holding a vial above a bowl to pour its liquid contents into it

Give the patient the entire contents of the container immediately.

If any of the mixture remains in the container, rinse the container with a small amount of water and give it to the patient to ensure complete ingestion.

Repeat this procedure each time the medication needs to be administered.

Infants under 1 year of age

To prepare a smaller single dose, you will need:

? One 45mg Tamiflu capsule

? A pair of sharp scissors

? Two small containers (use separate containers for each child)

? A large oral dosing dispenser to measure water—a 5 ml or 10 ml dispenser

? A small oral dosing dispenser marked in 0.1 ml increments to administer the dose

? A teaspoon (5 ml spoon)

? Water

? Sweetened food to mask the bitter taste of Tamiflu

Examples: chocolate syrup or cherry syrup, and dessert sauces such as caramel or condensed milk.

Alternatively, you may prepare sweetened water: mix one teaspoon of water with three-quarters (3/4) of a teaspoon of sugar.

Step 1: Pour all the powder into a container

Take one 45mg capsule and hold it vertically over one of the containers. Carefully cut off the rounded end with scissors. Be careful with the powder, as it may be irritating to the skin and eyes.

Pour all the powder into the container, regardless of the dose being prepared.

The amount is the same for both treatment and prevention of influenza.

Black line drawing showing a hand holding a pair of scissors cutting a small object held by another handLine drawing of a hand holding tweezers to dip an object into a glass bowl

Step 2: Add water to dilute the medication

Use the larger dispenser to draw up 7.5 ml of water.

Add the water to the powder in the container.

A hand holding a syringe with the liquid inside

Shake the suspension with a spoon for 2 minutes.

A hand immersing an object into a bowl with the text '2 mins' next to a circle with a vertical line indicating elapsed time

Do not worry if not all of the powder dissolves. The undissolved powder corresponds to inactive ingredients.

Step 3: Choose the correct amount for the child's weight

Find the child's weight in the left column of the table.

The right column of the table shows how much of the liquid mixture you will need to prepare.

Infants under 1 year of age (including full-term newborns)

Child's weight

(nearest)

Amount of mixture to prepare

3 kg

1.5 ml

3.5 kg

1.8 ml

4 kg

2.0 ml

4.5 kg

2.3 ml

5 kg

2.5 ml

5.5 kg

2.8 ml

6 kg

3.0 ml

6.5 kg

3.3 ml

7 kg

3.5 ml

7.5 kg

3.8 ml

8 kg

4.0 ml

8.5 kg

4.3 ml

9 kg

4.5 ml

9.5 kg

4.8 ml

10 kg or more

5.0 ml

Step 4: Prepare the liquid mixture

Make sure you have the correct dispenser size.

Prepare the correct amount of liquid mixture from the first container.

Prepare it carefully to avoid introducing air bubbles.

Gently add the correct dose to the second container.

Two hands carefully pouring the contents of a vial into a small transparent bowl containing liquidA hand holding a syringe with the liquid inside

Step 5: Sweeten and administer to the child

Add a small amount—no more than one teaspoon—of sweetened food to the second container.

This is to mask the bitter taste of the Tamiflu suspension.

Shake the sweetened food and Tamiflu liquid well.

Immediately give the child the entire contents of the second container (sweetened food mixed with the Tamiflu liquid).

If any mixture remains in the second container, rinse the container with a small amount of water and ensure the child drinks it all. For children unable to drink directly from the container, administer the remaining liquid using a spoon or an appropriate bottle.

Give the child something to drink.

Discard any remaining liquid left over from the first container.

Repeat this procedure each time the medication needs to be administered.


Information for healthcare professionals only

Patients unable to swallow capsules:

The marketed formulation of Tamiflu oral suspension (6 mg/ml) is the preferred medicine for pediatric and adult patients who have difficulty swallowing capsules or require lower doses. If Tamiflu oral suspension powder is not available, the pharmacist may prepare a suspension (6 mg/ml) from Tamiflu capsules. If pharmacy-prepared suspension is also unavailable, patients may prepare the suspension at home from capsules.

Oral dosing dispensers (oral syringes) with appropriate volume and graduations must be provided to administer the pharmacy-prepared suspension and for use in the home preparation procedures. In both cases, the required volumes should preferably be marked on the dispensers. For home preparation, dispensers must also be provided separately to measure the correct volume of water and to measure the Tamiflu-water mixture. To measure 5.0 ml of water, dispensers of 5 ml or 10 ml should be used.

The appropriate dispenser size for withdrawing the correct volume of Tamiflu suspension (6 mg/ml) is shown below.

Infants under 1 year of age (including full-term newborns):

Oseltamivir Dose

Amount of Oseltamivir Suspension

Syringe Size to Use (0.1 mL graduations)

9 mg

1.5 mL

2.0 mL (or 3.0 mL)

10 mg

1.7 mL

2.0 mL (or 3.0 mL)

11.25 mg

1.9 mL

2.0 mL (or 3.0 mL)

12.5 mg

2.1 mL

3.0 mL

13.75 mg

2.3 mL

3.0 mL

15 mg

2.5 mL

3.0 mL

16.25 mg

2.7 mL

3.0 mL

18 mg

3.0 mL

3.0 mL (or 5.0 mL)

19.5 mg

3.3 mL

5.0 mL

21 mg

3.5 mL

5.0 mL

22.5 mg

3.8 mL

5.0 mL

24 mg

4.0 mL

5.0 mL

25.5 mg

4.3 mL

5.0 mL

27 mg

4.5 mL

5.0 mL

28.5 mg

4.8 mL

5.0 mL

30 mg

5.0 mL

5.0 mL