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Cafiaspirina (Aspirin, Caffeine)

Active Ingredient: Aspirin, Caffeine
Dosage: 500 mg/50 mg
Route of Administration: Oral
Dosage Form: Tablets
Quantity per package: 100 tablets per pack
Availability: Out of stock

Cafiaspirina (acetylsalicylic acid + caffeine) is used for symptomatic relief of occasional mild or moderate pain, such as headaches, dental, menstrual, muscular (contractures) or back (lumbago). At the right moment, this drug is unavailable. Look for other pain relief options here.

Indications

  • Headache;
  • Painful contractures;
  • Dysmenorrhea;
  • Fever;
  • Low back pain;
  • Odontalgias.

Dosage and administration

Oral administration. Take the medication with meals, especially if digestive discomfort is observed. It should not be taken on an empty stomach. It is recommended to take a pill with plenty of liquid (water or milk).

Contraindications

  • Hypersensitivity to Cafiaspirina, caffeine, other salicylates, NSAIDs or tartrazine (cross-reaction);
  • Acute, chronic or recurrent gastroduodenal ulcer;
  • Gastric recurrence discomfort;
  • History of bleeding or gastric perforation after treatment;
  • Hemorrhagic diathesis;
  • A history of asthma;
  • Nasal polyps associated;
  • Coagulation disorders, mainly hemophilia or hypoprothrombinemia;
  • Concomitant use with oral anticoagulants;
  • Severe cardiovascular disorders;
  • Severe uncontrolled hypertension;
  • Children under 16 years old;
  • Reye’s Syndrome;
  • Third trimester of pregnancy.

Side effects

  • Increased risk of bleeding;
  • Perioperative bleeding;
  • Bruising;
  • Epistaxis;
  • Urogenital and/or gingival bleeding;
  • Hypoprothrombinemia (with high doses);
  • Paroxysmal bronchial spasm;
  • Severe dyspnea;
  • Rhinitis;
  • Asthma;
  • Nasal congestion;
  • Gastric ulcer;
  • Duodenal ulcer;
  • Gastrointestinal bleeding (melena, hematemesis);
  • Abdominal and gastrointestinal pain;
  • Dyspepsia;
  • Nausea;
  • Vomiting;
  • Hives;
  • Rashes;
  • Angioedema;
  • Pruritus;
  • Urticaria.

Overdose

No date reported.

Interaction

No date reported.

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