Grastek Sublingual Tablet 2800Bau Drug Medication Dosage Information
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GRASTEK: Sublingual tablet (2800BAU)

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GRASTEK 2800BAU Sub Tablet

What is this Medicine?

TIMOTHY GRASS POLLEN ALLERGEN EXTRACT (TIM uh thee gras POL en AL er jen EK strakt) is an allergy medicine. It is used to treat sneezing, runny or itchy nose, nasal congestion, and watery eyes caused by grass allergies.

CVS Pharmacy Patient Statistics for GRASTEK: Sublingual tablet(2800BAU)
Generic vs. Brand Name Usage*
*Brand contains same active ingredient but may not represent FDA-approved generic equivalent
Usage By Strength
In-Depth Information

GRASTEK 2800BAU Sublingual Tablet

NDC: 000064229
  • Prescription Required
  • Not a Controlled Drug
    (CSA Schedule)
  • FDA Approved




FDA approved for the following conditions:
Allergic Conjunctivitis, Allergic Rhinitis

Storage Information
Store in original package until time of use
Protect from moisture
Store between 68 to 77 degrees F, excursions permitted 59 to 86 degrees F
GRASTEK 2800BAU Sublingual Tablet

Reported Side Effects for GRASTEK 2800BAU Sublingual Tablet

Difficulty Swallowing Incidence:
1.0-2.0%*
Severity: MODERATE
Onset: DELAYED
Swelling Incidence:
1.0-11.1%*
Severity: MODERATE
Onset: DELAYED
Shortness Of Breath Incidence:
1.1-2.0%*
Severity: MODERATE
Onset: EARLY
Mouth Ulcers Incidence:
1.1-1.3%*
Severity: MODERATE
Onset: DELAYED
Hypoesthesia Incidence:
1.1-2.3%*
Severity: MILD
Onset: DELAYED
Inflamed Tongue Incidence:
1.3%*
Severity: MODERATE
Onset: EARLY
Tired Incidence:
1.4%*
Severity: MILD
Onset: EARLY
Skin Redness Incidence:
1.5-4.9%*
Severity: MODERATE
Onset: EARLY
Upset Stomach Incidence:
1.6-1.9%*
Severity: MILD
Onset: EARLY
Stuffy Nose Incidence:
1.6%*
Severity: MILD
Onset: EARLY
Sneezing Incidence:
1.6%*
Severity: MILD
Onset: EARLY
Chest Pain Incidence:
1.6-2.0%*
Severity: MODERATE
Onset: EARLY
Hives Incidence:
1.7-1.8%*
Severity: MILD
Onset: RAPID
Dry Mouth Incidence:
1.7%*
Severity: MILD
Onset: EARLY
Headache Incidence:
2.1-3.4%*
Severity: MILD
Onset: EARLY
Upset Stomach Incidence:
2.3%*
Severity: MILD
Onset: EARLY
Itching Incidence:
2.4-26.7%*
Severity: MILD
Onset: RAPID
Cough Incidence:
2.7%*
Severity: MILD
Onset: DELAYED
Itchy Eyes Incidence:
3.4%*
Severity: MILD
Onset: RAPID
Paresthesias Incidence:
5.4-9.8%*
Severity: MILD
Onset: DELAYED
Throat Irritation Incidence:
21.3-22.6%*
Severity: MILD
Onset: EARLY
*This is an approximate aggregated range of reported side effects from clinical studies performed on this drug. Your experience with this drug may be different.
Pregnancy & Lactation Information
FIRST Trimester

Class B - Animal studies have revealed no evidence of harm to the fetus, however, there are no adequate and well-controlled studies in pregnant women. OR Animal studies have shown an adverse effect, but adequate and well-controlled studies in pregnant women have failed to demonstrate a risk to the fetus in any trimester.

SECOND Trimester

Class B - Animal studies have revealed no evidence of harm to the fetus, however, there are no adequate and well-controlled studies in pregnant women. OR Animal studies have shown an adverse effect, but adequate and well-controlled studies in pregnant women have failed to demonstrate a risk to the fetus in any trimester.

THIRD Trimester

Class B - Animal studies have revealed no evidence of harm to the fetus, however, there are no adequate and well-controlled studies in pregnant women. OR Animal studies have shown an adverse effect, but adequate and well-controlled studies in pregnant women have failed to demonstrate a risk to the fetus in any trimester.

Lactation

Caution - Not enough information is available to rule out harm to infants when this drug is taken by nursing mothers.


Learning More About
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