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PACK IN HAND · ONE-PAGE CHECK

Medicine pack check sheet

Print this sheet or fill it in before speaking with a pharmacist or clinician. Copy only what is printed on the pack in hand. The published fields below are starting points from this record, not proof that your pack is the same product.

Published record starting point

Record display name
MEVALOTIN
Generic name / active ingredient
pravastatin sodium
Dosage-form class
Japan PMDA: pravastatin sodium 5 mg and 10 mg oral tablets; 0.5% and 1% oral fine granules (review the four product identities separately)
Route
Oral
Record reviewed
2026-08-30

Copy from the pack in hand

Source-linked reading points

  • The 5 mg and 10 mg tablets state an amount per tablet; the 0.5% and 1% granules state 5 mg or 10 mg per 1 g of granules. Percent, per-gram and per-tablet units cannot be directly converted from numbers on a webpage or used to calculate an individual's amount.
  • The PMDA label places pregnancy, possible pregnancy and breastfeeding within contraindication/important-use boundaries. When planning pregnancy, possibly pregnant, pregnant or breastfeeding, do not self-continue, stop, alternate days or switch statins from this page; contact the prescribing team or pharmacist promptly.
  • Unexplained muscle pain, tenderness, weakness or cramps, especially with marked fatigue, fever or dark urine, may need prompt medical assessment. The label includes serious muscle-injury warnings such as rhabdomyolysis. Do not wait for a webpage to decide whether a medicine caused the symptoms.
  • Liver or kidney problems, thyroid conditions, previous muscle reactions and a complete medicine list including fibrates, immunosuppressants or other lipid-lowering medicines may affect professional judgement. The site does not decide suitability, need for genetic testing or how to switch statins from one medicine name or laboratory result.

Reviewed presentation examples — compare every field

  • Pravastatin sodium 5 mg per tabletPMDA approval no. 21300AMZ00549
  • Pravastatin sodium 10 mg per tabletPMDA approval no. 20300AMZ00671
  • Pravastatin sodium 5 mg per 1 g of fine granules (0.5%)PMDA approval no. 21300AMZ00548
  • Pravastatin sodium 10 mg per 1 g of fine granules (1%)PMDA approval no. 20300AMZ00672

EDITORIAL RECORD

Who prepared and checked this page

Byline
OriginDrug Content Editorial
Review role
Public primary-source verification
Last reviewed
2026-08-30
Source record
4 clickable primary-source entry points are listed with this dossier.

The review role checks source traceability, stated market, document version and product-identity fields. It is not a claim of clinical licensure, prescribing authority or individual pharmacy service. Read the editorial policy.

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