pizensy
Pharmaranks rates Pizensy 3.5/5 for recall safety — an independent score from its FDA recall history and its manufacturer's record. Pizensy (Lactitol) is a medication supplied as a solution and for solution.
Lactitol · by Braintree
Based on 1 source · Recall-safety score from FDA recall history — this product's own recalls and its manufacturer's record. Not an efficacy or quality rating. methodology →
Key facts
Dosage forms
Solution
The forms currently marketed in the U.S., per the FDA National Drug Code Directory.
Ways to save
Ask for the generic
Same active ingredient, far cheaper. Is there a generic? →
Request a 90-day supply
Bulk fills usually lower the per-dose price vs monthly refills.
Use copay cards
Manufacturer copay cards & patient-assistance programs — especially for brand drugs.
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Frequently asked questions
- How is Pizensy rated?
- pharmaranks gives Pizensy a composite score of 3.5 out of 5, currently based on 1 weighted source (FDA regulatory recall-safety data weighted highest). See our methodology at /how-we-rate.
- Is there a coupon or discount for Pizensy?
- pharmaranks is an independent ratings site, not a pharmacy — we don't issue coupons or sell Pizensy. To pay less, ask your prescriber or pharmacist whether a generic equivalent exists, check the manufacturer's copay/savings card and patient-assistance program, and compare a pharmacy discount card against your insurance copay. Prices vary by pharmacy, insurance, and location, so always confirm at the counter. This is general reference, not medical or financial advice.
- Who makes Pizensy?
- Pizensy is marketed by Braintree. You can see Braintree's full profile, rating, and other products on pharmaranks.
- Is Pizensy a brand-name or generic drug?
- Pizensy is a brand-name product with the active ingredient Lactitol.
- Is Pizensy available over the counter?
- No. Pizensy is a prescription (Rx) medication in the US — you need a prescription from a licensed clinician (in person or via telehealth); it isn't sold over the counter. For some conditions there are OTC alternatives — ask your pharmacist.
- What forms does Pizensy come in?
- Pizensy is currently marketed as solution, per the FDA's National Drug Code Directory.
- Is Pizensy FDA-registered?
- Pizensy is on record with the U.S. FDA under application number NDA211281. You can verify this on its official FDA label.
- Has Pizensy been recalled by the FDA?
- Pizensy has no FDA recalls recorded under its own application in the openFDA enforcement database. Its recall-safety score reflects its manufacturer's overall recall record. This is general reference, not medical advice — check the FDA recall database for the latest alerts.
- Is Pizensy safe?
- There's no single safe-or-not verdict. pharmaranks gives Pizensy a recall-safety score of 70/100, based on its FDA recall history (no recalls under its own FDA application) — not an efficacy or side-effect rating. Review its FDA-label side effects and warnings before use, and always consult a licensed professional.
Information is sourced from public FDA regulatory data. Provided for general reference only — not medical advice. Always consult a licensed professional and the current prescribing information.
What people report to the FDA about LACTITOL
The FDA Adverse Event Reporting System (FAERS) collects reports from patients and clinicians. It holds 329 reports naming LACTITOL — the active ingredient in Pizensy, and the FDA flagged 97% of those reports as serious. The effects reported most often — leaving out reports about overdose, misuse or the condition being treated, which dominate the raw list for common medicines:
- hepatic encephalopathy20 reports
- asthenia17 reports
- hyponatraemia17 reports
- acute kidney injury15 reports
- fall15 reports
- dehydration14 reports
- febrile neutropenia12 reports
- general physical health deterioration12 reports
Read these as a signal, not a rate. A report does not mean LACTITOL caused the effect — anyone can file one, and many describe people taking several medicines for several conditions. Crucially there is no denominator: FAERS does not record how many people took the drug, so these counts cannot be turned into “X% of patients” — a bigger number often just means a more widely used or more talked-about drug. Duplicates exist, and publicity drives reporting. For what is actually established, read the FDA label.
Source: openFDA drug/event (FAERS), retrieved September 25, 2026.
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pizensy
70/100