Metformin Hcl side effects: what 55,016 FDA adverse event reports show
Drug class
Not stated in label
Brand names
Metformin Hydrochloride
Who reports
55,016 reports · 57% serious · 3,856 with death outcome · 56% female
Used for
Metformin hydrochloride extended-release tablets are indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus. Metformin hydrochloride extended-release tablets are a biguanide indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus. ( 1 )
What it is
Metformin hydrochloride extended-release tablets, USP contain the biguanidine antihyperglycemic agent, metformin, in the form of monohydrochloride salt.
Boxed warning
LACTIC ACIDOSIS Postmarketing cases of metformin-associated lactic acidosis have resulted in death, hypothermia, hypotension, and resistant bradyarrhythmias. The onset of metformin-associated lactic acidosis is often subtle, accompanied only by nonspecific symptoms such as malaise, myalgias, respiratory distress, somnolence, and abdominal pain.
Causality screen of the 40 strongest signals
What the badges mean
- Labeled — boxed warning The term (or its clinical synonym) appears in the FDA boxed warning: causality is regulator-recognised and considered serious.
- Labeled (related wording) The label describes this effect under different wording (e.g. 'neutropenia' for 'neutrophil count decreased'). Treated as known.
- Likely indication confounding The term appears in the label's indications: reports probably describe the disease being treated (or its progression), not a drug effect. Classic confounding by indication.
- Lab value / disease marker A laboratory result, investigation or disease-activity marker (antibody positive, CRP abnormal, swollen joint count) not described in the label. These usually mirror the monitored disease or testing protocol rather than a drug effect; not screened further.
- Not in label — unassessed Not found in the label text, not an artifact pattern. This is a genuine candidate for a formal causality assessment (Bradford Hill / WHO-UMC); it has NOT had one here.
Strongest disproportionality signals
Flagged terms (PRR ≥ 2, χ² ≥ 4, n ≥ 10), ranked by PRR; infinite PRRs (no comparator reports) excluded. The EBGM column is a second, shrinkage-based estimate (MGPS) with its 5th percentile EB05 and the BCPNN IC025; a pair flagged by PRR alone is marked PRR-only and should be read as fragile. The strata column recomputes the PRR on serious reports only (and, for the 300 most-reported drugs, adjusted for age band), and flags pairs whose reports are unusually skewed by sex or come mostly from consumers. Each row also shows the PRR against the other drugs of the same FDA class, which removes most confounding by the condition being treated, and a calibrated p-value: on validation, known non-causes average an ROR of about 2, so significance is judged against that empirical null (✓ = p < 0.05 after calibration). 1,150 further terms are in the interactive explorer. Reaction links open the term's cross-drug page.
| Reaction | Reports | PRR 95% CI · ROR · χ²/p | EBGM EB05 · IC025 | Label screen | Serious-only & strata | Trial cross-check |
|---|---|---|---|---|---|---|
| Continuous haemodiafiltration | 99 | 42.2 34.3–51.9ROR 42.3 · calibrated p 4e-5 ✓ | 37.8 EB05 31.9 · IC025 +4.7 3/3 methods agree | Not in label — unassessed | serious n=99 · 100% clinician | no trial arm names this drug |
| Early satiety | 189 | 41.9 36.0–48.7ROR 42.0 · calibrated p 4e-5 ✓ | 37.6 EB05 33.3 · IC025 +4.9 3/3 methods agree | Not in label — unassessed | 94% consumer | no trial arm names this drug |
| Lactic acidosis | 1,715 | 21.5 20.5–22.5ROR 22.1 · calibrated p 0.001 ✓ | 20.4 EB05 19.6 · IC025 +4.3 3/3 methods agree | Labeled — boxed warning exact term | serious PRR 20.3 | no trial arm names this drug |
| Haemodialysis | 381 | 17.9 16.1–19.8ROR 18.0 · calibrated p 0.003 ✓ | 17.1 EB05 15.7 · IC025 +3.9 3/3 methods agree | Labeled — boxed warning exact term | serious PRR 17.4 · 95% clinician | no trial arm names this drug |
| Renal failure acute | 1,831 | 16.9 16.1–17.7ROR 17.4 · calibrated p 0.004 ✓ | 16.2 EB05 15.6 · IC025 +3.9 3/3 methods agree | Labeled (related wording) related wording | serious PRR 16.4 | no trial arm names this drug |
| Blood glucose decreased | 2,034 | 16.8 16.0–17.5ROR 17.4 · calibrated p 0.004 ✓ | 16.1 EB05 15.5 · IC025 +3.9 3/3 methods agree | Labeled — boxed warning synonym match | serious PRR 8.0 · 87% consumer | no trial arm names this drug |
| Blood glucose fluctuation | 416 | 15.0 13.6–16.5ROR 15.1 · calibrated p 0.007 ✓ | 14.4 EB05 13.3 · IC025 +3.7 3/3 methods agree | Lab value / disease marker | serious n=139 · 82% consumer | no trial arm names this drug |
| Blood glucose increased | 6,972 | 14.6 14.2–14.9ROR 16.5 · calibrated p 0.005 ✓ | 14.0 EB05 13.8 · IC025 +3.8 3/3 methods agree | Lab value / disease marker | serious PRR 8.4 · 83% consumer | no trial arm names this drug |
| Anion gap increased | 49 | 14.4 10.8–19.2ROR 14.4 · calibrated p 0.009 ✓ | 13.7 EB05 10.7 · IC025 +3.1 3/3 methods agree | Labeled (related wording) related wording | serious n=48 · 100% clinician | no trial arm names this drug |
| Reflux oesophagitis | 28 | 14.4 9.9–21.0ROR 14.4 · calibrated p 0.011 ✓ | 13.5 EB05 9.5 · IC025 +2.9 3/3 methods agree | Not in label — unassessed | serious n=26 | no trial arm names this drug |
| Stomach discomfort | 187 | 14.1 12.2–16.3ROR 14.1 · calibrated p 0.009 ✓ | 13.6 EB05 12.0 · IC025 +3.5 3/3 methods agree | Not in label — unassessed | serious n=23 · 91% consumer | no trial arm names this drug |
| Medication residue | 89 | 13.4 10.8–16.5ROR 13.4 · calibrated p 0.012 ✓ | 12.9 EB05 10.7 · IC025 +3.3 3/3 methods agree | Not in label — unassessed | – | no trial arm names this drug |
| Acute prerenal failure | 37 | 12.4 8.9–17.2ROR 12.4 · calibrated p 0.017 ✓ | 11.6 EB05 8.6 · IC025 +2.8 3/3 methods agree | Labeled (related wording) related wording | serious n=37 | no trial arm names this drug |
| Anorexia | 387 | 11.6 10.5–12.8ROR 11.7 · calibrated p 0.019 ✓ | 11.2 EB05 10.3 · IC025 +3.3 3/3 methods agree | Not in label — unassessed | serious PRR 5.2 · 73% consumer | no trial arm names this drug |
| Hypoglycaemic coma | 84 | 11.4 9.2–14.1ROR 11.4 · calibrated p 0.022 ✓ | 10.9 EB05 9.0 · IC025 +3.0 3/3 methods agree | Not in label — unassessed | serious n=84 | no trial arm names this drug |
| Heart injury | 72 | 11.2 8.8–14.1ROR 11.2 · calibrated p 0.023 ✓ | 10.6 EB05 8.7 · IC025 +3.0 3/3 methods agree | Labeled (related wording) related wording | serious n=72 · ♀ 25% (drug 56%) | no trial arm names this drug |
| Joint sprain | 30 | 11.1 7.7–15.9ROR 11.1 · calibrated p 0.027 ✓ | 10.2 EB05 7.2 · IC025 +2.6 3/3 methods agree | Not in label — unassessed | serious n=21 · ♀ 100% (drug 56%) | no trial arm names this drug |
| Colonic polyp | 47 | 11.0 8.2–14.7ROR 11.0 · calibrated p 0.026 ✓ | 10.3 EB05 7.9 · IC025 +2.8 3/3 methods agree | Not in label — unassessed | serious n=45 | no trial arm names this drug |
| Diabetic neuropathy | 138 | 10.8 9.2–12.8ROR 10.9 · calibrated p 0.025 ✓ | 10.4 EB05 9.0 · IC025 +3.1 3/3 methods agree | Likely indication confounding shares a disease stem with the indications wording | serious n=126 | no trial arm names this drug |
| Diabetes mellitus inadequate control | 487 | 10.8 9.8–11.8ROR 10.8 · calibrated p 0.025 ✓ | 10.4 EB05 9.7 · IC025 +3.2 3/3 methods agree | Labeled (related wording) related wording | serious PRR 10.2 | no trial arm names this drug |
| Glycosylated haemoglobin increased | 655 | 10.2 9.4–11.0ROR 10.3 · calibrated p 0.030 ✓ | 9.9 EB05 9.3 · IC025 +3.2 3/3 methods agree | Lab value / disease marker | serious PRR 8.9 | no trial arm names this drug |
| Bladder transitional cell carcinoma | 36 | 9.8 7.0–13.6ROR 9.8 · calibrated p 0.039 ✓ | 9.0 EB05 6.6 · IC025 +2.5 3/3 methods agree | Not in label — unassessed | serious n=33 · ♀ 0% (drug 56%) · 100% clinician | no trial arm names this drug |
| Hypoglycaemia (low blood sugar) | 1,173 | 9.4 8.9–10.0ROR 9.6 · calibrated p 0.037 ✓ | 9.2 EB05 8.8 · IC025 +3.1 3/3 methods agree | Labeled — boxed warning exact term | serious PRR 8.6 | no trial arm names this drug |
| Blood amylase increased | 41 | 9.2 6.7–12.5ROR 9.2 · calibrated p 0.048 ✓ | 8.5 EB05 6.4 · IC025 +2.5 3/3 methods agree | Lab value / disease marker | serious n=38 | no trial arm names this drug |
| Sick sinus syndrome | 27 | 9.0 6.2–13.2ROR 9.0 · calibrated p 0.053 | 8.1 EB05 5.7 · IC025 +2.3 3/3 methods agree | Not in label — unassessed | serious n=27 | no trial arm names this drug |
| Ischaemic cardiomyopathy | 70 | 8.8 6.9–11.1ROR 8.8 · calibrated p 0.052 | 8.3 EB05 6.8 · IC025 +2.6 3/3 methods agree | Not in label — unassessed | serious n=71 · ♀ 30% (drug 56%) | no trial arm names this drug |
| Left atrial dilatation | 29 | 8.8 6.1–12.7ROR 8.8 · calibrated p 0.057 | 7.9 EB05 5.6 · IC025 +2.3 3/3 methods agree | Not in label — unassessed | serious n=29 | no trial arm names this drug |
| Cholecystitis chronic | 153 | 8.8 7.5–10.3ROR 8.8 · calibrated p 0.051 | 8.5 EB05 7.4 · IC025 +2.8 3/3 methods agree | Not in label — unassessed | serious PRR 8.6 · ♀ 100% (drug 56%) | no trial arm names this drug |
| Pancreatitis chronic | 53 | 8.8 6.7–11.5ROR 8.8 · calibrated p 0.054 | 8.2 EB05 6.4 · IC025 +2.5 3/3 methods agree | Not in label — unassessed | serious n=53 | no trial arm names this drug |
| Leukocytoclastic vasculitis | 37 | 8.7 6.3–12.1ROR 8.7 · calibrated p 0.057 | 8.0 EB05 6.0 · IC025 +2.4 3/3 methods agree | Not in label — unassessed | serious n=36 · 100% clinician | no trial arm names this drug |
| Pancreatitis acute | 477 | 8.3 7.6–9.1ROR 8.4 · calibrated p 0.058 | 8.1 EB05 7.5 · IC025 +2.9 3/3 methods agree | Not in label — unassessed | serious PRR 8.2 | no trial arm names this drug |
| Diabetic retinopathy | 70 | 8.0 6.3–10.1ROR 8.0 · calibrated p 0.070 | 7.6 EB05 6.2 · IC025 +2.5 3/3 methods agree | Likely indication confounding shares a disease stem with the indications wording | serious n=65 | no trial arm names this drug |
| High density lipoprotein decreased | 68 | 7.9 6.2–10.0ROR 7.9 · calibrated p 0.073 | 7.5 EB05 6.1 · IC025 +2.5 3/3 methods agree | Lab value / disease marker | serious n=48 | no trial arm names this drug |
| Cardioactive drug level increased | 27 | 7.9 5.4–11.5ROR 7.9 · calibrated p 0.079 | 7.0 EB05 5.0 · IC025 +2.1 3/3 methods agree | Lab value / disease marker | serious n=27 | no trial arm names this drug |
| Orthopnoea | 61 | 7.4 5.8–9.5ROR 7.4 · calibrated p 0.088 | 7.0 EB05 5.6 · IC025 +2.4 3/3 methods agree | Not in label — unassessed | serious n=61 · ♀ 35% (drug 56%) | no trial arm names this drug |
| Therapeutic agent toxicity | 63 | 7.2 5.6–9.3ROR 7.2 · calibrated p 0.095 | 6.8 EB05 5.5 · IC025 +2.3 3/3 methods agree | Not in label — unassessed | serious n=61 | no trial arm names this drug |
| Echocardiogram abnormal | 26 | 7.2 4.9–10.6ROR 7.2 · calibrated p 0.102 | 6.4 EB05 4.6 · IC025 +2.0 3/3 methods agree | Lab value / disease marker | serious n=26 | no trial arm names this drug |
| Metabolic syndrome | 30 | 7.1 4.9–10.1ROR 7.1 · calibrated p 0.106 | 6.4 EB05 4.6 · IC025 +2.1 3/3 methods agree | Labeled (related wording) related wording | serious n=23 · ♀ 100% (drug 56%) | no trial arm names this drug |
| Diabetic nephropathy | 40 | 7.0 5.1–9.6ROR 7.0 · calibrated p 0.107 | 6.4 EB05 4.9 · IC025 +2.2 3/3 methods agree | Likely indication confounding shares a disease stem with the indications wording | serious n=39 | no trial arm names this drug |
| Hypoglycaemic unconsciousness | 35 | 6.8 4.9–9.5ROR 6.8 · calibrated p 0.116 | 6.2 EB05 4.7 · IC025 +2.1 3/3 methods agree | Not in label — unassessed | serious n=34 · 100% consumer | no trial arm names this drug |
Trial evidence (ClinicalTrials.gov)
Most frequently reported reactions
By raw co-report count, regardless of disproportionality. Common terms here are often the illness itself or generic outcomes.
| Reaction | Reports | PRR 95% CI · ROR · χ²/p | EBGM EB05 · IC025 | Label screen | Serious-only & strata | Trial cross-check |
|---|---|---|---|---|---|---|
| Blood glucose increased | 6,972 | 14.6 14.2–14.9ROR 16.5 · calibrated p 0.005 ✓ | 14.0 EB05 13.8 · IC025 +3.8 3/3 methods agree | Lab value / disease marker | serious PRR 8.4 · 83% consumer | no trial arm names this drug |
| Nausea | 5,683 | 2.8 2.7–2.8ROR 3.0 · calibrated p 0.639 | 2.7 EB05 2.7 · IC025 +1.4 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 1.8 · 73% consumer | no trial arm names this drug |
| Weight decreased (weight loss) | 4,119 | 5.7 5.5–5.9ROR 6.1 · calibrated p 0.145 | 5.6 EB05 5.5 · IC025 +2.4 3/3 methods agree | Not in label — unassessed | serious PRR 2.7 · 80% consumer | no trial arm names this drug |
| Diarrhoea (diarrhea) | 3,580 | 2.1 2.1–2.2ROR 2.2 · calibrated p 0.948 | 2.1 EB05 2.1 · IC025 +1.0 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 1.9 | no trial arm names this drug |
| Vomiting | 2,958 | 2.4 2.3–2.5ROR 2.5 · calibrated p 0.816 | 2.4 EB05 2.3 · IC025 +1.2 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 2.0 | no trial arm names this drug |
| Drug ineffective (drug did not work) | 2,556 | 0.7 0.7–0.8ROR 0.7 · calibrated p 0.144 | 0.7 EB05 0.7 · IC025 -0.5 PRR-only: not supported by EBGM or IC | Reporting / coding artifact | serious PRR 0.7 · 72% consumer | no trial arm names this drug |
| Fatigue (tiredness) | 2,446 | 1.2 1.2–1.2ROR 1.2 · calibrated p 0.447 | 1.2 EB05 1.2 · IC025 +0.2 | Not in label — unassessed | serious PRR 1.2 | no trial arm names this drug |
| Dizziness | 2,287 | 1.8 1.7–1.8ROR 1.8 · calibrated p 0.822 | 1.8 EB05 1.7 · IC025 +0.7 | Labeled adverse reaction exact term | serious PRR 1.6 | no trial arm names this drug |
| Decreased appetite (loss of appetite) | 2,255 | 3.7 3.6–3.9ROR 3.9 · calibrated p 0.406 | 3.7 EB05 3.6 · IC025 +1.8 3/3 methods agree | Not in label — unassessed | serious PRR 1.6 · 81% consumer | no trial arm names this drug |
| Blood glucose decreased | 2,034 | 16.8 16.0–17.5ROR 17.4 · calibrated p 0.004 ✓ | 16.1 EB05 15.5 · IC025 +3.9 3/3 methods agree | Labeled — boxed warning synonym match | serious PRR 8.0 · 87% consumer | no trial arm names this drug |
| Dyspnoea (shortness of breath) | 1,924 | 1.3 1.2–1.4ROR 1.3 · calibrated p 0.514 | 1.3 EB05 1.2 · IC025 +0.3 | Not in label — unassessed | serious PRR 1.5 | no trial arm names this drug |
| Headache | 1,919 | 1.2 1.1–1.2ROR 1.2 · calibrated p 0.423 | 1.2 EB05 1.1 · IC025 +0.1 | Labeled adverse reaction exact term | serious PRR 1.1 | no trial arm names this drug |
| Renal failure acute | 1,831 | 16.9 16.1–17.7ROR 17.4 · calibrated p 0.004 ✓ | 16.2 EB05 15.6 · IC025 +3.9 3/3 methods agree | Labeled (related wording) related wording | serious PRR 16.4 | no trial arm names this drug |
| Asthenia (weakness) | 1,803 | 1.8 1.8–1.9ROR 1.9 · calibrated p 0.865 | 1.8 EB05 1.8 · IC025 +0.8 | Not in label — unassessed | serious PRR 1.7 | no trial arm names this drug |
| Lactic acidosis | 1,715 | 21.5 20.5–22.5ROR 22.1 · calibrated p 0.001 ✓ | 20.4 EB05 19.6 · IC025 +4.3 3/3 methods agree | Labeled — boxed warning exact term | serious PRR 20.3 | no trial arm names this drug |
Unlabeled candidate signals
These flagged terms were not found in the FDA label text and do not match an artifact pattern. They are the pairs that would merit a structured assessment (temporality, dose-response, biological plausibility, consistency across databases, trial or cohort evidence). The screen has not done that; string-matching misses label wording, and a strong PRR can still be stimulated reporting, co-medication, or the disease itself.
- Continuous haemodiafiltration — n=99, PRR 42.2
- Early satiety — n=189, PRR 41.9
- Reflux oesophagitis — n=28, PRR 14.4
- Stomach discomfort — n=187, PRR 14.1
- Medication residue — n=89, PRR 13.4
- Anorexia — n=387, PRR 11.6
- Hypoglycaemic coma — n=84, PRR 11.4
- Joint sprain — n=30, PRR 11.1
- Colonic polyp — n=47, PRR 11.0
- Bladder transitional cell carcinoma — n=36, PRR 9.8
✓ A hand-written Bradford Hill causality assessment exists for this drug: Metformin ↔ Lactic acidosis.
Want to assess one of these properly? The runbook describes the Bradford Hill / trial-evidence workflow used on the assessment page, and handoff_top1000_signals.csv lists the strongest unassessed pairs across all drugs.
Common questions
What are the most reported side effects of Metformin Hcl?
In FDA FAERS, the most frequently co-reported reaction terms for Metformin Hcl are blood glucose increased, nausea, weight decreased, diarrhoea, vomiting, fatigue. These are report counts, not rates: FAERS has no denominator, reporting is voluntary and uneven, and a term can be reported because of the illness being treated rather than the drug.
Does Metformin Hcl have an FDA boxed warning?
Yes. The current FDA label carries a boxed warning: LACTIC ACIDOSIS Postmarketing cases of metformin-associated lactic acidosis have resulted in death, hypothermia, hypotension, and resistant bradyarrhythmias. The onset of metformin-associated lactic acidosis is often subtle, accompanied only by nonspecific symptoms such as malaise, myalgias, respiratory distress, somnolence, and abdominal pain.
Do FAERS signals prove that Metformin Hcl causes these side effects?
No. A disproportionality signal (PRR, ROR) means a reaction is reported more often with this drug than with others in the database. That can reflect a real effect, but also the disease being treated, stimulated reporting after news or litigation, co-medications, or how reports are coded. Causality needs temporality, dose-response, biological plausibility, consistency across data sources and, ideally, trial or cohort evidence. This page screens each term against the FDA label and ClinicalTrials.gov results; it does not establish causation.
Sources & methods
- FDA label via openFDA (set ID 7e41818c-60e9-4bcf-9586-7bb8d33d5e89, effective 20260615; matched on
openfda.generic_name.exact:"METFORMIN") - Bayesian shrinkage measures computed offline over all 1,317,300 cached pairs: BCPNN information component (IC, with Norén closed-form IC025) and MGPS empirical-Bayes geometric mean (EBGM, EB05) with a two-component gamma prior fitted by maximum marginal likelihood (α₁=0.57, β₁=0.02, α₂=1.42, β₂=0.70, w=0.17); unstratified
- FAERS pair statistics from the OpenPV build of 2026-09-14 (openFDA
count=aggregation, fieldpatient.drug.openfda.generic_name.exact, 1,190 reaction terms, min 3 co-reports); PRR/ROR with 95% CI, chi-square with Yates correction - Serious-only and stratified counts (serious:1, patient.patientsex, primarysource.qualification) from openFDA count queries; serious-only PRR uses the drug serious report total and the term global serious total (N_serious=11,882,979); strata shown only when n ≥ 20
- Seriousness and sex counts from openFDA
count=serious,patient.patientsex,seriousnessdeath - ClinicalTrials.gov API v2 (query
METFORMIN, results-bearing studies sorted by enrollment)
Page generated 2026-10-14. Label and PubChem text are retrieved automatically and may lag the current label; always check the current prescribing information. OpenPV is a beta research tool of the Open Source Medicine Foundation.