CHAMGAP
Verdict No. 3088 · Search date 2026-09-15 · Methodology v1.0

Added riboflavin,
does it really help with Hemoglobin increase in anemic pregnant women receiving iron and folate?

30-Second Summary
C
Evidence Grade C · 46 · Safety unknown
ChatGPT source review and self-verification · Codex technical integration
This is a current-value judgment. Uncertainties are disclosed and new verified material will trigger documented revision. The score is a Chamgap rule-based index, not a probability of success.
The existence of a pregnancy study does not establish safety across doses and formulations. Arm-level adverse-event denominators and long-term maternal/fetal outcomes were not verified in the accessed material. This is not advice to stop shared iron–folate treatment or replace it with B2.
What the
research shows
Human studies adding B2 to iron and folate in anemic pregnant women were identified. However, the precise Hb increment and precision for B2 alone could not be separately verified from currently accessible material, giving C·46. This is not treated as no research or no effect, nor generalized to treatment of all anemia.
What the
ads claim
Advertising and mechanistic claims were not used as grade bonuses or direct clinical evidence.

Four separate assessment dimensions

Effect direction and sizeHuman studies adding B2 to iron and folate in anemic pregnant women were identified. However, the precise Hb increment and precision for B2 alone could not be separately verified from currently accessible material, giving C·46. This is not treated as no research or no effect, nor generalized to treatment of all anemia.
Evidence certaintyHb is a surrogate (S). The decisive randomized trial supporting the principal contrast is R1; unverified funding is I1 under precedent 29. The B2-only treatment magnitude is not currently verified (EX, CX), and short duration gives B1. The supplied calculator returns C, with 0 strength axes giving the fixed score of 46.
ApplicabilityPregnant women selected for anemia by Hb; not all confirmed to have iron-deficiency anemia
SafetyThe existence of a pregnancy study does not establish safety across doses and formulations. Arm-level adverse-event denominators and long-term maternal/fetal outcomes were not verified in the accessed material. This is not advice to stop shared iron–folate treatment or replace it with B2.

Not official GRADE or treatment-success probability; ? has no score.

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Useful facts when choosing a product

  • The target question concerns oral supplementation. Ma’s abstract specifies supplement amounts and arms but not an explicit route or detailed dosage form, so the actual study route is not filled in as a verified fact. The oral question and unconfirmed observed route are separated in structured fields.
ID

Chamgap Semantic Classification Code

Permanent code issued

S.riboflavin.oral-addon.anemic-pregnancy-hemoglobin.increase.addon

Supplements > Added riboflavin > Oral add-on > Hemoglobin in anemic pregnancy > Increase claim > Added to common iron and folate

Technically bound to the current-value claim boundary fixed by ChatGPT. Unconfirmed dose, duration, study details, and evidence grade remain in verdict fields and revision history rather than the permanent semantic code. The code identifies the intervention and claim; it never contains the evidence grade, score, or safety result.

Download semantic index (JSON) · Codebook v1

Exact Claim Classification

These independent facets prevent evidence from different forms, routes, populations, effects, and comparators from being mixed.

Intervention classS · Supplement or nutraceutical
Canonical ingredient or interventionAdded riboflavin (vitamin B2)
Source or part usedSynthetic/fermentation/other production origin unconfirmed; plant-part classification not applicable
Formulation or processingSupplement comparison adding B2 alone; detailed dosage form/release profile unconfirmed in the decisive abstract
RouteOral (page question; see observed_evidence for study-route verification)
DosePrincipal question: B2 1.0 mg/day added; 5 mg from another study not pooled
DurationPrincipal question: 2 months; longer-term/postpartum persistence unconfirmed
PopulationPregnant women selected for anemia by Hb; not all confirmed to have iron-deficiency anemia
Effect or conditionHemoglobin increase in anemic pregnant women receiving iron and folate
Primary endpointBetween-group difference in blood Hb change; distinct from anemia prevalence and combined-nutrient effects
ComparatorMatched iron 60 mg/day and folic acid 400 μg/day; excludes vitamin A add-on arms
Duplicate-detection keyriboflavin-addon|oral|1mg-day|2months|anemic-pregnancy-on-iron-folate|hemoglobin-change|iron-60mg-folate-400ug-background
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What the research actually shows

The principal contrast is IFB versus IF in Ma’s trial, isolating the arm that added only B2 to shared iron and folate. The abstract’s 5.4±1.1 g/L belongs to IFAB versus IF, which added vitamin A as well as B2, and is not adopted as the B2-only increment. Hb-defined anemia is not assumed to establish iron deficiency in every participant.

02

Why this is classified as C (46)

Hb is a surrogate (S). The decisive randomized trial supporting the principal contrast is R1; unverified funding is I1 under precedent 29. The B2-only treatment magnitude is not currently verified (EX, CX), and short duration gives B1. The supplied calculator returns C, with 0 strength axes giving the fixed score of 46.

Counterpoint. Suprapto’s study used alternating allocation and excluded participants from analysis. Its significant abstract comparison was the B2 arm versus the vitamin A arm, not confirmed B2 benefit versus iron–folate alone. RIBOFEM’s low-B2 healthy-woman population and sample-size assumptions are not used as observed treatment effects for the present anemia question.

Rejudgment record. Human studies adding B2 to iron and folate in anemic pregnant women were identified. However, the precise Hb increment and precision for B2 alone could not be separately verified from currently accessible material, giving C·46. This is not treated as no research or no effect, nor generalized to treatment of all anemia. — Hb is a surrogate (S). The decisive randomized trial supporting the principal contrast is R1; unverified funding is I1 under precedent 29. The B2-only treatment magnitude is not currently verified (EX, CX), and short duration gives B1. The supplied calculator returns C, with 0 strength axes giving the fixed score of 46.

Stored scoring profile
EndpointSSurrogate marker - laboratory or imaging measures
Case application: S: Hb laboratory endpoint
ReplicationR1Single confirmatory trial
Case application: R1: decisive Ma contrast; different-dose alternating-allocation study not verified independent replication of the exact contrast
IndependenceI1Mixed funding sources
Case application: I1: funding not obtained, precedent 29
Effect sizeEXThe clinical size of the effect could not be judged
Case application: EX: IFB–IF Hb magnitude not verified; combined vitamin A+B2 contrast excluded
PrecisionCXNo pooled confidence interval could be confirmed
Case application: CX: IFB–IF CI not verified

Stored derived and displayed grades match; this is not a current recalculation or validity check (C).

Review performed and remaining limitations

Self-checked directly accessed material, provided records and stated arithmetic as of the cutoff; not independent external review.

Complete cause-specific classification of Hb-defined anemia unconfirmed Actual route and detailed dosage form not stated in the decisive accessed abstract IFB–IF Hb difference, dispersion, interval and analysis denominator unconfirmed Full text could not be obtained through the linked source Native databases worldwide were not exhaustively searched; the current judgment is published with that limitation.

Search scope and limitations. tasks/R01-006/search_log.json

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Evidence Table

StudyDesignSampleFundingEndpointResultWeight
Ma et al. — retinol/riboflavin added to iron and folate in anemic pregnant women (2008)Randomized double-blind four-arm trial; B2 add-on contrast IFB–IF366 assigned overall; IFB 91, IF 93; Hb analysis denominator unconfirmedUnconfirmed or not used in this page gradeHb and anemia prevalence in anemic pregnant women; registered primary designation unverifiedIFB–IF Hb magnitude and dispersion for B2 alone remain unconfirmed; the vitamin A+B2 combination estimate is not transferredDecisive result with explicitly unconfirmed route details
Suprapto et al. — riboflavin added to iron–folate in anemic pregnant women (2002)Alternating allocation; not asserted to be randomizedOnly verified denominators are recorded in numeric_evidence.json; assignment totals are not substituted for unknown endpoint analysis counts.Unconfirmed or not used in this page gradeHb in anemic pregnant women; alternating allocation and multiple comparisonsThe study alternately allocated 103 pregnant participants. Riboflavin (B2) was 5 mg for 60 days; 19 participants (reported 18.4%) were excluded from analysis.Indirect contextual evidence
RIBOFEM protocol — riboflavin status and hematology in young womenExcluded: different population and protocol, not resultsOnly verified denominators are recorded in numeric_evidence.json; assignment totals are not substituted for unknown endpoint analysis counts.Unconfirmed or not used in this page gradeHematology protocol in healthy women with low B2 status, not observed resultsRIBOFEM recruited healthy young women with low B2 status. A Hb difference used for sample-size planning is not an observed treatment result.Excluded: different population and protocol, not results
Correcting marginal riboflavin deficiency and hematologic status in young UK women (2011)Same-trial candidate; outcome details not verifiedOnly verified denominators are recorded in numeric_evidence.json; assignment totals are not substituted for unknown endpoint analysis counts.Unconfirmed or not used in this page gradeHematology result paper in healthy women; no current full-text effect value adoptedPrior bibliography/access record reused; no unverified effect estimate adopted.Same-trial candidate; outcome details not verified
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Receipt — 4 References

Evidence access cutoff: 2026-09-15. Each citation states its actual access level (full-text transcription, abstract, index, or other) and remaining limitations. Bibliographic checking does not certify the study results or treatment efficacy.

Ma et al. — retinol/riboflavin added to iron and folate in anemic pregnant women (2008)
The anemia trial assigned 366 pregnant participants to four arms. The B2-only add-on arm IFB had 91 participants and the iron–folate arm IF had 93. Read with the recorded access level and location; not a claim that inaccessible full text was reviewed.
checked
Suprapto et al. — riboflavin added to iron–folate in anemic pregnant women (2002)
The study alternately allocated 103 pregnant participants. Riboflavin (B2) was 5 mg for 60 days; 19 participants (reported 18.4%) were excluded from analysis. Read with the recorded access level and location; not a claim that inaccessible full text was reviewed.
checked
RIBOFEM protocol — riboflavin status and hematology in young women
RIBOFEM recruited healthy young women with low B2 status. A Hb difference used for sample-size planning is not an observed treatment result. Read with the recorded access level and location; not a claim that inaccessible full text was reviewed.
checked
Correcting marginal riboflavin deficiency and hematologic status in young UK women (2011)
Prior record reused; not verification of a current effect estimate. Read with the recorded access level and location; not a claim that inaccessible full text was reviewed.
checked
Pregnant women selected for anemia by Hb; not all confirmed to have iron-deficiency anemia
Technical integration by: Codex · Evidence date: 2026-09-15 · Corrections: 2

Correction log — 2

Corrections applied to this verdict, in chronological order. Changes are logged, not erased.

  • 2026-09-15 · current_value_initial_publication — 5.4±1.1 g/L was excluded as an isolated B2 effect. The unspecified dispersion type was not filled in as SD or SE.
  • 2026-09-15 · current_value_initial_publication — Alternating allocation was not labeled randomization; a sample-size assumption was not used as an observed Hb increase.

Cite this verdict

Added riboflavin (vitamin B2) × Hemoglobin increase in anemic pregnant women receiving iron and folate Evidence Grade C card
[Chamgap] Added riboflavin (vitamin B2) × Hemoglobin increase in anemic pregnant women receiving iron and folate — Evidence Grade C·46. 4 cited sources checked. Source: https://chamgap.com/en/verdicts/energy/riboflavin-addon-anemic-pregnancy-hemoglobin/ · CC BY 4.0

CC BY 4.0 — free to use with attribution; do not distort grades, numbers, or verdict meaning.

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What this document does and does not do

Chamgap is an information source. It reports what research has and has not confirmed; it does not tell readers what to take or buy. That decision belongs to readers and, when needed, medical or legal professionals. This verdict reflects literature available up to the search date and may change as new research appears. Nothing here is medical advice.