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Exakte Wirkstoffkennungen und zitierbare Passagen zu Wechselwirkungen, Gegenanzeigen und Nebenwirkungen.

Ein Paarvergleich findet Originalpassagen, die den anderen Wirkstoff wörtlich nennen. Aussagen gelten für das jeweilige Präparat und seine Formulierung. Klassenbegriffe und abweichende Synonyme können fehlen. Kein Treffer bedeutet nicht, dass keine Wechselwirkung besteht.

RxNorm 05-Oct-2026 · geprüft 2026-10-25 · 1009 Präparate · 54812 Quellenpassagen · 148 strukturierte Aussagen. Automatisch aktualisiert, ohne menschliche Freigabe.

Pioglitazone Actavis

HOS-155342 · Fachinformation

Quellenpassagen (12)

Gegenanzeigen · Pioglitazone Actavis

Pioglitazone Actavis 15 mg tablets Pioglitazone Actavis 30 mg tablets Pioglitazone Actavis 45 mg tablets · Abschnitt 4.3 · PDF-Seite 4

HOS-214485 · Präparat HOS-155342

Pioglitazone is contraindicated in patients with:

Originalpassage; keine automatisch abgeleitete Schwere, Häufigkeit oder Kausalität. Auch verneinte Befunde und nicht untersuchte Kombinationen bleiben sichtbar.

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Version 2023-06-01T02:00:00Z · SHA-256 ad23e703c99e588d5e3753a426a2d517a2d2fd35bbce3778e82f258ef487d9a7 · Passage c5eaecae7a87b8afc633eb0ab49fd0bda0064de506b8893659e601e381e0997c · Zeichen 0–49 im Abschnitt

Gegenanzeigen · Pioglitazone Actavis

Pioglitazone Actavis 15 mg tablets Pioglitazone Actavis 30 mg tablets Pioglitazone Actavis 45 mg tablets · Abschnitt 4.3 · PDF-Seite 4

HOS-214486 · Präparat HOS-155342

- hypersensitivity to the active substance or to any of the excipients - cardiac failure or history of cardiac failure (NYHA stages I to IV) - hepatic impairment - diabetic ketoacidosis - current bladder cancer or a history of bladder cancer - uninvestigated macroscopic haematuria.

Originalpassage; keine automatisch abgeleitete Schwere, Häufigkeit oder Kausalität. Auch verneinte Befunde und nicht untersuchte Kombinationen bleiben sichtbar.

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Version 2023-06-01T02:00:00Z · SHA-256 ad23e703c99e588d5e3753a426a2d517a2d2fd35bbce3778e82f258ef487d9a7 · Passage 017b7f81b24794f882235e20de1bdce956ef594afa602c6379df196327411c66 · Zeichen 51–357 im Abschnitt

Wechselwirkungen · Pioglitazone Actavis

Pioglitazone Actavis 15 mg tablets Pioglitazone Actavis 30 mg tablets Pioglitazone Actavis 45 mg tablets · Abschnitt 4.5 · PDF-Seite 6

HOS-214487 · Präparat HOS-155342

Interaction studies have shown that pioglitazone has no relevant effect on either the pharmacokinetics or pharmacodynamics of digoxin, warfarin, phenprocoumon and metformin. Co-administration of pioglitazone with sulphonylureas does not appear to affect the pharmacokinetics of the sulphonylurea. Studies in man suggest no induction of the main inducible cytochrome P450, 1A, 2C8/9 and 3A4. In vitro studies have shown no inhibition of any subtype of cytochrome P450. Interactions with substances metabolised by these enzymes, e.g. oral contraceptives, cyclosporin, calcium channel blockers, and HMGCoA reductase inhibitors are not to be expected.

Originalpassage; keine automatisch abgeleitete Schwere, Häufigkeit oder Kausalität. Auch verneinte Befunde und nicht untersuchte Kombinationen bleiben sichtbar.

RxNorm-Namen im Text (wörtliche Treffer, Rolle nicht bewertet): digoxin (HOS-086172) phenprocoumon (HOS-091031) calcium (HOS-085615) warfarin (HOS-085950) metformin (HOS-091032)

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Version 2023-06-01T02:00:00Z · SHA-256 ad23e703c99e588d5e3753a426a2d517a2d2fd35bbce3778e82f258ef487d9a7 · Passage 85cf85e270341e1f6e4c76ef9e007a4e2939afc6caf970ffcd8a8245b8364d15 · Zeichen 0–647 im Abschnitt

Wechselwirkungen · Pioglitazone Actavis

Pioglitazone Actavis 15 mg tablets Pioglitazone Actavis 30 mg tablets Pioglitazone Actavis 45 mg tablets · Abschnitt 4.5 · PDF-Seite 6

HOS-214488 · Präparat HOS-155342

Co-administration of pioglitazone with gemfibrozil (an inhibitor of cytochrome P450 2C8) is reported to result in a 3-fold increase in AUC of pioglitazone. Since there is a potential for an increase in dose-related adverse events, a decrease in the dose of pioglitazone may be needed when gemfibrozil is concomitantly administered. Close monitoring of glycaemic control should be considered (see section 4.4). Co-administration of pioglitazone with rifampicin (an inducer of cytochrome P450 2C8) is reported to result in a 54% decrease in AUC of pioglitazone. The pioglitazone dose may need to be

Originalpassage; keine automatisch abgeleitete Schwere, Häufigkeit oder Kausalität. Auch verneinte Befunde und nicht untersuchte Kombinationen bleiben sichtbar.

RxNorm-Namen im Text (wörtliche Treffer, Rolle nicht bewertet): gemfibrozil (HOS-088403)

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Version 2023-06-01T02:00:00Z · SHA-256 ad23e703c99e588d5e3753a426a2d517a2d2fd35bbce3778e82f258ef487d9a7 · Passage a52f283e660089fed2c52035123a7e98b25ef1d98de008dfa152cc1cb651291d · Zeichen 649–1245 im Abschnitt

Wechselwirkungen · Pioglitazone Actavis

Pioglitazone Actavis 15 mg tablets Pioglitazone Actavis 30 mg tablets Pioglitazone Actavis 45 mg tablets · Abschnitt 4.5 · PDF-Seite 6–7

HOS-214489 · Präparat HOS-155342

6 increased when rifampicin is concomitantly administered. Close monitoring of glycaemic control should be considered (see section 4.4).

Originalpassage; keine automatisch abgeleitete Schwere, Häufigkeit oder Kausalität. Auch verneinte Befunde und nicht untersuchte Kombinationen bleiben sichtbar.

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Version 2023-06-01T02:00:00Z · SHA-256 ad23e703c99e588d5e3753a426a2d517a2d2fd35bbce3778e82f258ef487d9a7 · Passage eeb644ea00124ff9c0823af900b841d8308e3aafcd39f3f3be1276c31b993bf9 · Zeichen 1299–1436 im Abschnitt

Nebenwirkungen · Pioglitazone Actavis

Pioglitazone Actavis 15 mg tablets Pioglitazone Actavis 30 mg tablets Pioglitazone Actavis 45 mg tablets · Abschnitt 4.8 · PDF-Seite 7

HOS-214490 · Präparat HOS-155342

Adverse reactions reported in excess (> 0.5%) of placebo and as more than an isolated case in patients receiving pioglitazone in double-blind studies are listed below as MedDRA preferred term by system organ class and absolute frequency. Frequencies are defined as: very common (≥1/10); common (≥1/100 to <1/10); uncommon (≥1/1,000 to <1/100); rare (≥1/10,000 to <1/1,000); very rare (<1/10,000); not known (cannot be estimated from the available data). Within each frequency grouping, adverse reactions are presented in order of decreasing incidence and seriousness.

Originalpassage; keine automatisch abgeleitete Schwere, Häufigkeit oder Kausalität. Auch verneinte Befunde und nicht untersuchte Kombinationen bleiben sichtbar.

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Version 2023-06-01T02:00:00Z · SHA-256 ad23e703c99e588d5e3753a426a2d517a2d2fd35bbce3778e82f258ef487d9a7 · Passage 0812046abd33153b8d3145ca05e2f4ae031f288b2ab9c54d826d088881b242f1 · Zeichen 0–567 im Abschnitt

Nebenwirkungen · Pioglitazone Actavis

Pioglitazone Actavis 15 mg tablets Pioglitazone Actavis 30 mg tablets Pioglitazone Actavis 45 mg tablets · Abschnitt 4.8 · PDF-Seite 7

HOS-214491 · Präparat HOS-155342

Frequency of adverse reactions of pioglitazone by treatment regimen Combination Adverse with reaction Mono- with with sulpho- metformin therapy with insulin metformin nylurea and sulpho- nylurea Infections and infestations upper respiratory common common common common common tract infection bronchitis common sinusitis uncommon uncommon uncommon uncommon uncommon Blood and lymphatic system disorders anaemia common

Originalpassage; keine automatisch abgeleitete Schwere, Häufigkeit oder Kausalität. Auch verneinte Befunde und nicht untersuchte Kombinationen bleiben sichtbar.

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Version 2023-06-01T02:00:00Z · SHA-256 ad23e703c99e588d5e3753a426a2d517a2d2fd35bbce3778e82f258ef487d9a7 · Passage 6e75d39f4530d017c2fc4bcc611db3ef5cb34ce44ce5078cd384649e3d49128d · Zeichen 594–1623 im Abschnitt

Nebenwirkungen · Pioglitazone Actavis

Pioglitazone Actavis 15 mg tablets Pioglitazone Actavis 30 mg tablets Pioglitazone Actavis 45 mg tablets · Abschnitt 4.8 · PDF-Seite 7–8

HOS-214492 · Präparat HOS-155342

7 Frequency of adverse reactions of pioglitazone by treatment regimen Combination Adverse with reaction Mono- with with sulpho- metformin therapy with insulin metformin nylurea and sulpho- nylurea Immune System Disorders Hypersensitivity not known not known not known not known not known and allergic reactions1 Metabolism and nutrition disorders uncommon very common hypo-glycaemia common appetite increased uncommon Nervous system disorders hypo-aesthesia common common common common common headache common uncommon dizziness common insomnia uncommon uncommon uncommon uncommon uncommon Eye disorders visual common common uncommon disturbance2 macular oedema not known not known not known not known not known Ear and labyrinth disorders vertigo uncommon Cardiac disorders heart failure3 common Neoplasms benign, malignant and unspecified (including cysts and polyps) bladder cancer uncommon uncommon uncommon uncommon uncommon Respiratory, thoracic and mediastinal disorders dyspnoea common Gastrointestinal disorders flatulence uncommon common

Originalpassage; keine automatisch abgeleitete Schwere, Häufigkeit oder Kausalität. Auch verneinte Befunde und nicht untersuchte Kombinationen bleiben sichtbar.

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Version 2023-06-01T02:00:00Z · SHA-256 ad23e703c99e588d5e3753a426a2d517a2d2fd35bbce3778e82f258ef487d9a7 · Passage 5f4194269d26f43a1f36cb586d0aea78d0b0eaeac6ad4fc682c4a1acffe78f16 · Zeichen 1678–3747 im Abschnitt

Nebenwirkungen · Pioglitazone Actavis

Pioglitazone Actavis 15 mg tablets Pioglitazone Actavis 30 mg tablets Pioglitazone Actavis 45 mg tablets · Abschnitt 4.8 · PDF-Seite 8–9

HOS-214493 · Präparat HOS-155342

8 Frequency of adverse reactions of pioglitazone by treatment regimen Combination Adverse with reaction Mono- with with sulpho- metformin therapy with insulin metformin nylurea and sulpho- nylurea Skin and subcutaneous tissue disorders sweating uncommon Musculoskeletal and connective tissue disorders fracture bone4 common common common common common arthralgia common common common back pain common Renal and urinary disorders haematuria common glycosuria uncommon proteinuria uncommon Reproductive system and breast disorders erectile common dysfunction General disorders and administration site conditions oedema5 very common fatigue uncommon Investigations weight increased6 common common common common common blood creatine common phospho-kinase increased increased lactic uncommon dehydro-genase Alanine not known not known not known not known not known aminotransferase increased7

Originalpassage; keine automatisch abgeleitete Schwere, Häufigkeit oder Kausalität. Auch verneinte Befunde und nicht untersuchte Kombinationen bleiben sichtbar.

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Version 2023-06-01T02:00:00Z · SHA-256 ad23e703c99e588d5e3753a426a2d517a2d2fd35bbce3778e82f258ef487d9a7 · Passage c37afdd47beaad7ce5de5f679e6bf009cf8538c983af9dc718e07d2d02dc32d3 · Zeichen 3799–5833 im Abschnitt

Nebenwirkungen · Pioglitazone Actavis

Pioglitazone Actavis 15 mg tablets Pioglitazone Actavis 30 mg tablets Pioglitazone Actavis 45 mg tablets · Abschnitt 4.8 · PDF-Seite 9

HOS-214494 · Präparat HOS-155342

Description of selected adverse reactions 1 Postmarketing reports of hypersensitivity reactions in patients treated with pioglitazone have been reported. These reactions include anaphylaxis, angioedema, and urticaria. 2 Visual disturbance has been reported mainly early in treatment and is related to changes in blood glucose due to temporary alteration in the turgidity and refractive index of the lens as seen with other hypoglycaemic treatments.

Originalpassage; keine automatisch abgeleitete Schwere, Häufigkeit oder Kausalität. Auch verneinte Befunde und nicht untersuchte Kombinationen bleiben sichtbar.

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Version 2023-06-01T02:00:00Z · SHA-256 ad23e703c99e588d5e3753a426a2d517a2d2fd35bbce3778e82f258ef487d9a7 · Passage a34233e805b36ddd3279be454a82af5ba438208533bc3c1cc0cb4849c2f6ac87 · Zeichen 5835–6285 im Abschnitt

Nebenwirkungen · Pioglitazone Actavis

Pioglitazone Actavis 15 mg tablets Pioglitazone Actavis 30 mg tablets Pioglitazone Actavis 45 mg tablets · Abschnitt 4.8 · PDF-Seite 9–10

HOS-214495 · Präparat HOS-155342

9 3 In controlled clinical trials the incidence of reports of heart failure with pioglitazone treatment was the same as in placebo, metformin and sulphonylurea treatment groups, but was increased when used in combination therapy with insulin. In an outcome study of patients with pre-existing major macrovascular disease, the incidence of serious heart failure was 1.6% higher with pioglitazone than with placebo, when added to therapy that included insulin. However, this did not lead to an increase in mortality in this study. In this study in patients receiving pioglitazone and insulin, a higher percentage of patients with heart failure was observed in patients aged ≥65 years compared with those less than 65 years (9.7% compared to 4.0%). In patients on insulin with no pioglitazone the incidence of heart failure was 8.2% in those ≥65 years compared to 4.0% in patients less than 65 years. Heart failure has been reported with marketing use of pioglitazone, and more frequently when pioglitazone was used in combination with insulin or in patients with a history of cardiac failure. 4 A pooled analysis was conducted of adverse reactions of bone fractures from randomised, comparator controlled, double blind clinical trials in over 8100 patients in the pioglitazone-treated groups and 7400 in the comparator-treated groups of up to 3.5 years duration. A higher rate of fractures was observed in women taking pioglitazone (2.6%) versus comparator (1.7%). No increase in fracture rates was observed in men treated with pioglitazone (1.3%) versus comparator (1.5%). In the 3.5 year PROactive study, 44/870 (5.1%) of pioglitazone-treated female patients experienced fractures compared to 23/905 (2.5%) of female patients treated with comparator. No increase in fracture rates was observed in men treated with pioglitazone (1.7%) versus comparator (2.1%). Post- marketing, bone fractures have been reported in both male and female patients (see section 4.4). 5 Oedema was reported in 6–9% of patients treated with pioglitazone over one year in controlled clinical trials. The oedema rates for comparator groups (sulphonylurea, metformin) were 2–5%. The reports of oedema were generally mild to moderate and usually did not require discontinuation of treatment. 6 In active comparator controlled trials mean weight increase with pioglitazone given as monotherapy was 2–3 kg over one year. This is similar to that seen in a sulphonylurea active comparator group. In combination trials pioglitazone added to metformin resulted in mean weight increase over one year of 1.5 kg and added to a sulphonylurea of 2.8 kg. In comparator groups, addition of sulphonylurea to metformin resulted in a mean weight gain of 1.3 kg and addition of metformin to a sulphonylurea a mean weight loss of 1.0 kg. 7 In clinical trials with pioglitazone the incidence of elevations of ALT greater than three times the upper limit of normal was equal to placebo but less than that seen in metformin or sulphonylurea comparator groups. Mean levels of liver enzymes decreased with treatment with pioglitazone. Rare cases of elevated liver enzymes and hepatocellular dysfunction have occurred in post-marketing experience. Although in very rare cases fatal outcome has been reported, causal relationship has not been established.

Originalpassage; keine automatisch abgeleitete Schwere, Häufigkeit oder Kausalität. Auch verneinte Befunde und nicht untersuchte Kombinationen bleiben sichtbar.

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Version 2023-06-01T02:00:00Z · SHA-256 ad23e703c99e588d5e3753a426a2d517a2d2fd35bbce3778e82f258ef487d9a7 · Passage 5e5925d9830fcad0c9cf0faf67c8f93e1ede99c1a6dfd6c1a2b74c0f397739cc · Zeichen 6340–9650 im Abschnitt

Nebenwirkungen · Pioglitazone Actavis

Pioglitazone Actavis 15 mg tablets Pioglitazone Actavis 30 mg tablets Pioglitazone Actavis 45 mg tablets · Abschnitt 4.8 · PDF-Seite 10

HOS-214496 · Präparat HOS-155342

Reporting of suspected adverse reactions Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions via the national reporting system listed in Appendix V.

Originalpassage; keine automatisch abgeleitete Schwere, Häufigkeit oder Kausalität. Auch verneinte Befunde und nicht untersuchte Kombinationen bleiben sichtbar.

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Version 2023-06-01T02:00:00Z · SHA-256 ad23e703c99e588d5e3753a426a2d517a2d2fd35bbce3778e82f258ef487d9a7 · Passage 42f7144177697b690f59b1bda795c3fd216297691cf296a2e1269a137feab3cd · Zeichen 9652–10007 im Abschnitt

This product uses publicly available data from the U.S. National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services; NLM is not responsible for the product and does not endorse or recommend this or any other product.