Meruvax II Side Effects
Generic Name: rubella virus vaccine
Note: This page contains information about the side effects of rubella virus vaccine. Some of the dosage forms included on this document may not apply to the brand name Meruvax II.
Not all side effects for Meruvax II may be reported. You should always consult a doctor or healthcare professional for medical advice. Side effects can be reported to the FDA here.
For the Consumer
Applies to rubella virus vaccine: subcutaneous injectable, subcutaneous powder for solution
In addition to its needed effects, some unwanted effects may be caused by rubella virus vaccine (the active ingredient contained in Meruvax II). In the event that any of these side effects do occur, they may require medical attention.
You should check with your doctor immediately if any of these side effects occur when taking rubella virus vaccine:Symptoms of allergic reaction
- Difficulty in breathing or swallowing
- itching, especially of feet or hands
- reddening of skin, especially around ears
- swelling of eyes, face, or inside of nose
- unusual tiredness or weakness (sudden and severe)
If any of the following side effects occur while taking rubella virus vaccine, check with your doctor or nurse as soon as possible:Less common
- Pain or tenderness of eyes
- Bruising or purple spots on skin
- convulsions (seizures)
- headache (severe or continuing)
- pain, numbness, or tingling of hands, arms, legs, or feet
- stiff neck
- unusual irritability
Some of the side effects that can occur with rubella virus vaccine may not need medical attention. As your body adjusts to the medicine during treatment these side effects may go away. Your health care professional may also be able to tell you about ways to reduce or prevent some of these side effects. If any of the following side effects continue, are bothersome or if you have any questions about them, check with your health care professional:More common
- Burning or stinging at place of injection
- skin rash
- swelling of glands in neck
- Aches or pain in joints
- headache (mild), sore throat, runny nose, or fever
- itching, swelling, redness, tenderness, or hard lump at place of injection
- vague feeling of bodily discomfort
The above side effects (especially aches or pain in joints) are more likely to occur in adults, particularly women.
Some of the above side effects may not occur until 1 to 4 weeks after immunization and usually last less than 1 week. Aches or pain in joints may not occur until 1 to 10 weeks after immunization, and usually lasts less than 1 week. Check with your doctor if this side effect continues or is bothersome.
For Healthcare Professionals
Applies to rubella virus vaccine: subcutaneous powder for injection
Local side effects have included injection site burning/stinging, wheal and flare, erythema, pain, and induration.
Hypersensitivity reactions have included anaphylaxis, anaphylactoid reactions, angioneurotic edema (including peripheral or facial edema), and bronchial spasm.
Cardiovascular side effects have included vasculitis.
Dermatologic side effects have included Stevens-Johnson Syndrome, erythema multiforme, urticaria, and rash.
Gastrointestinal side effects have included pancreatitis; diarrhea, vomiting, and nausea.
Hematologic side effects have included thrombocytopenia, purpura, regional lymphadenopathy, and leukocytosis.
Musculoskeletal side effects have included arthralgia and/or arthritis (usually transient and rarely chronic), myalgia, paresthesia, and rarely chronic arthritis; these symptoms may also occur with natural rubella.
The vaccine has rarely been associated with chronic joint symptoms. The incidence of arthritis and arthralgia is generally higher in adult women than in children (women, 12% to 26%; children, 0% to 3%), and symptoms tend to be more marked and of longer duration, persisting for months or years (rare). In adolescent girls, the incidence of reactions appears to be intermediate between those seen in children and in women. These reactions are generally well tolerated and rarely interfere with normal activities, even in women over 35 years old.
Nervous system side effects have included encephalitis, Guillain-Barré Syndrome (GBS), polyneuritis, polyneuropathy, and paresthesia.
Ocular side effects have included optic neuritis, papillitis, retrobulbar neuritis, and conjunctivitis.
Otic side effects have included nerve deafness and otitis media.
Respiratory side effects have included sore throat, cough, and rhinitis.
A postmarketing surveillance study of measles/mumps/rubella vaccine in Finland during 1982 to 1993 with 1.5 million pediatric and adult vaccinees reported no deaths or permanent sequelae.
Other side effects have included fever, syncope, headache, dizziness, malaise, and irritability. Fatalities have been reported with the polyvalent measles/mumps/rubella vaccine; however, causality has not been determined.
Health care providers should report any allergic or unusual adverse reactions to the Vaccine Adverse Event Reporting System (VAERS) at 1-800-822-7967 (USA) and the manufacturer.
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