FDA records indicate that there are no current recalls for this drug.
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Moisturizing Lubricant Eye Drops Recall
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Questions & Answers
Side Effects & Adverse Reactions
- for external use only
- to avoid contamination, do not touch tip of container to any surface. Replace cap after using
- if solution changes color or becomes cloudy, do not use
- you feel eye pain
- changes in vision
- continued redness or irritation of the eye(s) gets worse, persists or lasts more than 72 hours
If swallowed, get medical help or contact a Poison Control Center right away.
- you feel eye pain
- changes in vision
- continued redness or irritation of the eye(s) gets worse, persists or lasts more than 72 hours
Legal Issues
There is currently no legal information available for this drug.
FDA Safety Alerts
There are currently no FDA safety alerts available for this drug.
Manufacturer Warnings
There is currently no manufacturer warning information available for this drug.
FDA Labeling Changes
There are currently no FDA labeling changes available for this drug.
Uses
- for the temporary relief of burning irritation and discomfort due to dryness of the eye or exposure to the wind and sun
- may be used as a protectant against further irritation
History
There is currently no drug history available for this drug.
Other Information
There are no additional details available for this product.
Sources
Moisturizing Lubricant Eye Drops Manufacturers
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Premier Value
Moisturizing Lubricant Eye Drops | Afaxys Inc.
To achieve maximum contraceptive effectiveness, CyredTM must be taken exactly as directed and at intervals not exceeding 24 hours. CyredTM is available in a blister pack which is printed for a Sunday Start. Day 1 Start is also provided.
Day 1 Start
The dosage of CyredTM for the initial cycle of therapy is one white "active" tablet administered daily from the 1st day through the 21st day of the menstrual cycle, counting the first day of menstrual flow as "Day 1". Tablets are taken without interruption as follows: One white "active" tablet daily for 21 days, then one green "reminder" tablet daily for 7 days. After 28 tablets have been taken, a new course is started and a white "active" tablet is taken the next day.
The use of CyredTM for contraception may be initiated 4 weeks postpartum in women who elect not to breastfeed. When the tablets are administered during the postpartum period, the increased risk of thromboembolic disease associated with the postpartum period must be considered. (See CONTRAINDICATIONS and WARNINGS concerning thromboembolic disease. See also PRECAUTIONS: Nursing Mothers.) If the patient starts on CyredTM postpartum, and has not yet had a period, she should be instructed to use another method of contraception until a white "active" tablet has been taken daily for 7 days. The possibility of ovulation and conception prior to initiation of medication should be considered. If the patient misses one (1) white "active" tablet in Weeks 1, 2, or 3, the white "active" tablet should be taken as soon as she remembers. If the patient misses two (2) white "active" tablets in Week 1 or Week 2, the patient should take two (2) white "active" tablets the day she remembers and two (2) white "active" tablets the next day; and then continue taking one (1) white "active" tablet a day until she finishes the pack. The patient should be instructed to use a back-up method of birth control such as a condom or spermicide if she has sex in the seven (7) days after missing pills. If the patient misses two (2) white "active" tablets in the third week or misses three (3) or more white "active" tablets in a row, the patient should throw out the rest of the pack and start a new pack that same day. The patient should be instructed to use a back-up method of birth control if she has sex in the seven (7) days after missing pills.
Sunday Start
When taking CyredTM, the first white "active" tablet should be taken on the first Sunday after menstruation begins. If the period begins on Sunday, the first white "active" tablet is taken on that day. If switching directly from another oral contraceptive, the first white "active" tablet should be taken on the first Sunday after the last ACTIVE tablet of the previous product. Tablets are taken without interruption as follows: One white "active" tablet daily for 21 days, then one green "reminder" tablet daily for 7 days. After 28 tablets have been taken, a new course is started and a white "active" tablet is taken the next day (Sunday). When initiating a Sunday start regimen, another method of contraception should be used until after the first 7 consecutive days of administration.
The use of CyredTM for contraception may be initiated 4 weeks postpartum. When the tablets are administered during the postpartum period, the increased risk of thromboembolic disease associated with the postpartum period must be considered. (See CONTRAINDICATIONS and WARNINGS concerning thromboembolic disease. See also PRECAUTIONS: Nursing Mothers.) If the patient starts on CyredTM postpartum, and has not yet had a period, she should be instructed to use another method of contraception until a white "active" tablet has been taken daily for 7 days. The possibility of ovulation and conception prior to initiation of medication should be considered. If the patient misses one (1) white active tablet in Weeks 1, 2, or 3, the white "active" tablet should be taken as soon as she remembers. If the patient misses two (2) white "active" tablets in Week 1 or Week 2, the patient should take two (2) white "active" tablets the day she remembers and two (2) white "active" tablets the next day; and then continue taking one (1) white "active" tablet a day until she finishes the pack. The patient should be instructed to use a back-up method of birth control such as a condom or spermicide if she has sex in the seven (7) days after missing pills. If the patient misses two (2) white "active" tablets in the third week or misses three (3) or more white "active" tablets in a row, the patient should continue taking one white "active" tablet every day until Sunday. On Sunday the patient should throw out the rest of the pack and start a new pack that same day. The patient should be instructed to use a back-up method of birth control if she has sex in the seven (7) days after missing pills.
ADDITIONAL INSTRUCTIONS FOR ALL DOSING REGIMENS
Breakthrough bleeding, spotting, and amenorrhea are frequent reasons for patients discontinuing oral contraceptives. In breakthrough bleeding, as in all cases of irregular bleeding from the vagina, nonfunctional causes should be borne in mind. In undiagnosed persistent or recurrent abnormal bleeding from the vagina, adequate diagnostic measures are indicated to rule out pregnancy or malignancy. If pathology has been excluded, time or a change to another formulation may solve the problem. Changing to an oral contraceptive with a higher estrogen content, while potentially useful in minimizing menstrual irregularity, should be done only if necessary since this may increase the risk of thromboembolic disease.
Use of oral contraceptives in the event of a missed menstrual period:
If the patient has not adhered to the prescribed schedule, the possibility of pregnancy should be considered at the time of the first missed period and oral contraceptive use should be discontinued if pregnancy is confirmed. If the patient has adhered to the prescribed regimen and misses two consecutive periods, pregnancy should be ruled out.
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