Nurofen® 200 mg coated tablets are a medicine containing the active ingredient ibuprofen, which has a pronounced analgesic, anti-inflammatory and antipyretic effect.
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Nurofen® 200 mg coated tablets are a medicine containing the active ingredient ibuprofen, which has pronounced analgesic, anti-inflammatory and antipyretic effects.
Indications:
- Pain conditions (e.g. back pain, toothache, muscle pain, joint pain, period pain, nerve pain)
- For the treatment of the acute headache phase in migraine with or without aura, and for the treatment of tension-type headaches
- Pain associated with colds and flu-like infections.
If you do not feel any better, or if your condition worsens, after the following number of days, please consult your doctor:
- in adolescents after 3 days
- for adults, after 3 days of fever or after 4 days of pain.
Dosage form
Coated tablets
Directions for use
- Adults and adolescents over 12 years of age: Follow the recommended dosage exactly. Start treatment with 1–2 coated tablets. Thereafter, take a further 1–2 coated tablets every 4 hours as required. However, do not take more than 6 coated tablets (1,200 mg) per day! Stop taking the medicine once your symptoms have subsided.
- Use in children and adolescents: Nurofen must only be given to children under 12 years of age on medical prescription.
- Method of administration: For oral use and for short-term treatment only. Swallow the coated tablets whole with sufficient liquid.
- Duration of use: If adolescents need to take this medicine for more than 3 days, or if their symptoms worsen, medical advice should be sought. If your symptoms worsen or do not improve after 3 days (in the case of fever) or after 4 days (in the case of pain), you should consult a doctor.
Ingredients
- The active ingredient is: ibuprofen. 1 coated tablet contains 200 mg of ibuprofen.
- The other ingredients are: Tablet core: croscarmellose sodium, sodium dodecyl sulphate, sodium citrate, stearic acid, highly dispersed silicon dioxide; Tablet coating: sodium carmellose, talc, gum arabic, sucrose, titanium dioxide (E 171), macrogol 6000; printing ink: Opacode black, consisting of: shellac, black iron oxide (E 172), vegetable lecithin (soya), Antifoam DC 1510 or Black Printing Ink consisting of: shellac, black iron oxide (E 172), propylene glycol.
| Alcohol-free: | Not specified |
|---|---|
| Gluten-free: | Not specified |
| Lactose-free: | Not specified |
| Perfume: | Not specified |
| Piece: | 24 |
| Sugar-free: | Not specified |
| Vegan: | Not specified |
Instructions for use
| Type of use: | Unzerkaut mit Flüssigkeit einnehmen |
|---|---|
| Field of use: | Leichte bis mäßig starke Schmerzzustände; - Akuten Kopfschmerzphase bei Migräne mit und ohne Aura, Spannungskopfschmerzen; - Schmerzen bei Erkältungskrankheiten und grippalen Infekten |
| Dosage: | Möglichst kurzzeitig und niedrig dosiert anwenden Bei Bedarf initial 1-2 Dragees, MTD 6 Dragees 1200 mg Für Kinder unter 12 Jahren nur auf ärztliche Verschreibung |
| Properties and efficacy: | Nichtsteroidales Antiphlogistikum |
| Contraindications: | LogImport.sisx.GAD.Akute MagenDarm-Ulcera, Blutungen oder Perforationen oder in Anamnese, Analgetika-Asthma, aktive Blutungen, ungeklärte Blutbildungsstörungen, starke Dehydrierung, schwere Herz-, Leber- oder Niereninsuffizienz |
| Side effects: | Überempfindlichkeitsreaktionen, MagenDarm abdominale Schmerzen, Blutungen, Ulzera, Perforation, ZNS Kopfschmerzen, Sehstörungen aseptische Meningitis, schwere Hautreaktionen TEN, Stevens-Johnson-Syndrom, AGEP, Niereninsuffizienz, Öde |
| Special warnings for safe use: | Vorsicht bei Risikofaktoren für kardiovaskuläre Ereignisse, Hypertonie, Porphyrie, chronisch entzündlichen Darmerkrankungen, Allergikern, Lupus erythematodes, Mischkollagenosen, nach größeren chirurgischen Eingriffen Bei Langzeitanwe |
| Interactions: | ASS und andere NSARs vermeiden Vorsicht Verstärkung Gerinnungshemmer, Kortikoide Blutungsrisiko, Sulfonylharnstoffe, Methotrexat, Phenytoin, Digoxin, Lithium, SSRIs, kaliumsparende Diuretika, Alkohol Verminderung Diuretika, andere An |
| Pregnancy and breastfeeding period: | Gegenanzeige im 3 Trimenon, sonst strenge Indikationsstellung Bei Kurzzeitanwendung Stillen möglich |
Pregnancy information
| Use forbidden |
|---|
| Use only if absolutely or vitally indicated |
Breastfeeding information
| Breastfeeding only if absolutely or vitally indicated |
|---|
| Breastfeeding possible under careful supervision |
Pictograms
| Caution for diabetics |
|---|
| Take intact |
| Avoid alcohol intake |