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VICTIM PRODUCT REPLACEMENT PROGRAM Administration Form By checking this box, the named Participant confirms that the Participant has (i) contacted Emergent Travel Health Medical Information at medical
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How to fill out vivotif - fda prescribing

01
To fill out Vivotif as per FDA prescribing, follow these steps:
02
Begin by reading the patient information leaflet provided with Vivotif.
03
Take Vivotif on an empty stomach, at least one hour before or two hours after a meal.
04
Swallow the capsule whole with a cold or lukewarm drink. Do not chew or crush the capsule.
05
Avoid taking any antacids, antibiotics, or substances that make your stomach less acidic within the 24 hours before and after taking Vivotif.
06
Store Vivotif in the refrigerator, and protect it from light.
07
Complete the full course of Vivotif as prescribed by your healthcare provider, even if you feel better.
08
If you miss a dose, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and continue with your regular dosing schedule.
09
Do not take extra doses of Vivotif to make up for missed doses.
10
If you have any questions or concerns about taking Vivotif, consult your healthcare provider or pharmacist.

Who needs vivotif - fda prescribing?

01
Vivotif is recommended for individuals who require protection against typhoid fever caused by Salmonella typhi bacteria.
02
It is mainly indicated for those traveling to areas where typhoid fever is endemic or highly prevalent.
03
The vaccine is particularly important for travelers to developing countries with limited access to safe drinking water and proper sanitation.
04
Individuals who will be in close contact with typhoid fever patients or working in environments with increased risk of exposure to the bacteria may also need Vivotif.
05
However, it is essential to consult a healthcare provider to determine if Vivotif is suitable for your specific situation.
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Vivotif is a vaccine used to prevent typhoid fever, which is approved by the FDA and requires specific prescribing information.
Healthcare providers who prescribe the Vivotif vaccine are required to file the associated FDA prescribing information.
To fill out the Vivotif FDA prescribing information, providers must complete the designated forms with accurate patient and vaccination details, ensuring compliance with FDA guidelines.
The purpose of Vivotif FDA prescribing is to provide essential information regarding the vaccine's usage, dosage, and potential side effects to ensure safe patient administration.
The information that must be reported includes patient demographics, vaccination history, dosage, administration route, and any adverse effects experienced post-vaccination.
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