Faster access than browser!Similarities between Analgesic and Ibuprofen
Analgesic and Ibuprofen have 36 things in common (in Unionpedia): Acetone, Antipyretic, Aspirin, Constipation, Cyclooxygenase, CYP2C9, Dexibuprofen, Dichloromethane, Diclofenac, Dysmenorrhea, Ethanol, Fever, Flurbiprofen, Hypertension, Indometacin, Inflammation, Intravenous therapy, Juvenile idiopathic arthritis, Ketoprofen, Methanol, Migraine, Myocardial infarction, Naproxen, Nausea, Nonsteroidal anti-inflammatory drug, Osteoarthritis, Over-the-counter drug, Pain, Paracetamol, Patent ductus arteriosus, ..., Renal colic, Rheumatoid arthritis, Stevens–Johnson syndrome, Stroke, Toxic epidermal necrolysis, Vomiting. Expand index (6 more) »
Acetone
Acetone (systematically named propanone) is the organic compound with the formula (CH3)2CO.
Acetone and Analgesic · Acetone and Ibuprofen ·
Antipyretic
Antipyretics (from anti- 'against' and 'feverish') are substances that reduce fever.
Analgesic and Antipyretic · Antipyretic and Ibuprofen ·
Aspirin
Aspirin, also known as acetylsalicylic acid (ASA), is a medication used to treat pain, fever, or inflammation.
Analgesic and Aspirin · Aspirin and Ibuprofen ·
Constipation
Constipation refers to bowel movements that are infrequent or hard to pass.
Analgesic and Constipation · Constipation and Ibuprofen ·
Cyclooxygenase
Cyclooxygenase (COX), officially known as prostaglandin-endoperoxide synthase (PTGS), is an enzyme (specifically, a family of isozymes) that is responsible for formation of prostanoids, including thromboxane and prostaglandins such as prostacyclin, from arachidonic acid.
Analgesic and Cyclooxygenase · Cyclooxygenase and Ibuprofen ·
CYP2C9
Cytochrome P450 2C9 (abbreviated CYP2C9) is an enzyme that in humans is encoded by the CYP2C9 gene.
Analgesic and CYP2C9 · CYP2C9 and Ibuprofen ·
Dexibuprofen
Dexibuprofen is a nonsteroidal anti-inflammatory drug (NSAID).
Analgesic and Dexibuprofen · Dexibuprofen and Ibuprofen ·
Dichloromethane
Methylene dichloride (DCM, or methylene chloride, or dichloromethane) is a geminal organic compound with the formula CH2Cl2.
Analgesic and Dichloromethane · Dichloromethane and Ibuprofen ·
Diclofenac
Diclofenac (sold under a number of trade names) is a nonsteroidal anti-inflammatory drug (NSAID) taken or applied to reduce inflammation and as an analgesic reducing pain in certain conditions.
Analgesic and Diclofenac · Diclofenac and Ibuprofen ·
Dysmenorrhea
Dysmenorrhea, also known as painful periods, or menstrual cramps, is pain during menstruation.
Analgesic and Dysmenorrhea · Dysmenorrhea and Ibuprofen ·
Ethanol
Ethanol, also called alcohol, ethyl alcohol, grain alcohol, and drinking alcohol, is a chemical compound, a simple alcohol with the chemical formula.
Analgesic and Ethanol · Ethanol and Ibuprofen ·
Fever
Fever, also known as pyrexia and febrile response, is defined as having a temperature above the normal range due to an increase in the body's temperature set-point.
Analgesic and Fever · Fever and Ibuprofen ·
Flurbiprofen
Flurbiprofen is a member of the phenylalkanoic acid derivative family of nonsteroidal anti-inflammatory drugs (NSAIDs).
Analgesic and Flurbiprofen · Flurbiprofen and Ibuprofen ·
Hypertension
Hypertension (HTN or HT), also known as high blood pressure (HBP), is a long-term medical condition in which the blood pressure in the arteries is persistently elevated.
Analgesic and Hypertension · Hypertension and Ibuprofen ·
Indometacin
Indometacin (INN; or USAN indomethacin) is a nonsteroidal anti-inflammatory drug (NSAID) commonly used as a prescription medication to reduce fever, pain, stiffness, and swelling from inflammation.
Analgesic and Indometacin · Ibuprofen and Indometacin ·
Inflammation
Inflammation (from inflammatio) is part of the complex biological response of body tissues to harmful stimuli, such as pathogens, damaged cells, or irritants, and is a protective response involving immune cells, blood vessels, and molecular mediators.
Analgesic and Inflammation · Ibuprofen and Inflammation ·
Intravenous therapy
Intravenous therapy (IV) is a therapy that delivers liquid substances directly into a vein (intra- + ven- + -ous).
Analgesic and Intravenous therapy · Ibuprofen and Intravenous therapy ·
Juvenile idiopathic arthritis
Juvenile idiopathic arthritis (JIA), also known as juvenile rheumatoid arthritis, is the most common form of arthritis in children and adolescents.
Analgesic and Juvenile idiopathic arthritis · Ibuprofen and Juvenile idiopathic arthritis ·
Ketoprofen
Ketoprofen, (RS)-2-(3-benzoylphenyl)-propionic acid (chemical formula C16H14O3) is one of the propionic acid class of nonsteroidal anti-inflammatory drugs (NSAID) with analgesic and antipyretic effects.
Analgesic and Ketoprofen · Ibuprofen and Ketoprofen ·
Methanol
Methanol, also known as methyl alcohol among others, is a chemical with the formula CH3OH (a methyl group linked to a hydroxyl group, often abbreviated MeOH).
Analgesic and Methanol · Ibuprofen and Methanol ·
Migraine
A migraine is a primary headache disorder characterized by recurrent headaches that are moderate to severe.
Analgesic and Migraine · Ibuprofen and Migraine ·
Myocardial infarction
Myocardial infarction (MI), commonly known as a heart attack, occurs when blood flow decreases or stops to a part of the heart, causing damage to the heart muscle.
Analgesic and Myocardial infarction · Ibuprofen and Myocardial infarction ·
Naproxen
Naproxen (brand names: Aleve, Naprosyn, and many others) is a nonsteroidal anti-inflammatory drug (NSAID) of the propionic acid class (the same class as ibuprofen) that relieves pain, fever, swelling, and stiffness.
Analgesic and Naproxen · Ibuprofen and Naproxen ·
Nausea
Nausea or queasiness is an unpleasant sense of unease, discomfort, and revulsion towards food.
Analgesic and Nausea · Ibuprofen and Nausea ·
Nonsteroidal anti-inflammatory drug
Nonsteroidal anti-inflammatory drugs (NSAIDs) are a drug class that reduce pain, decrease fever, prevent blood clots and, in higher doses, decrease inflammation.
Analgesic and Nonsteroidal anti-inflammatory drug · Ibuprofen and Nonsteroidal anti-inflammatory drug ·
Osteoarthritis
Osteoarthritis (OA) is a type of joint disease that results from breakdown of joint cartilage and underlying bone.
Analgesic and Osteoarthritis · Ibuprofen and Osteoarthritis ·
Over-the-counter drug
Over-the-counter (OTC) drugs are medicines sold directly to a consumer without a prescription from a healthcare professional, as opposed to prescription drugs, which may be sold only to consumers possessing a valid prescription.
Analgesic and Over-the-counter drug · Ibuprofen and Over-the-counter drug ·
Pain
Pain is a distressing feeling often caused by intense or damaging stimuli.
Analgesic and Pain · Ibuprofen and Pain ·
Paracetamol
--> Acetanilide was the first aniline derivative serendipitously found to possess analgesic as well as antipyretic properties, and was quickly introduced into medical practice under the name of Antifebrin by A. Cahn and P. Hepp in 1886. But its unacceptable toxic effects, the most alarming being cyanosis due to methemoglobinemia, prompted the search for less toxic aniline derivatives. Harmon Northrop Morse had already synthesised paracetamol at Johns Hopkins University via the reduction of ''p''-nitrophenol with tin in glacial acetic acid in 1877, but it was not until 1887 that clinical pharmacologist Joseph von Mering tried paracetamol on humans. In 1893, von Mering published a paper reporting on the clinical results of paracetamol with phenacetin, another aniline derivative. Von Mering claimed that, unlike phenacetin, paracetamol had a slight tendency to produce methemoglobinemia. Paracetamol was then quickly discarded in favor of phenacetin. The sales of phenacetin established Bayer as a leading pharmaceutical company. Overshadowed in part by aspirin, introduced into medicine by Heinrich Dreser in 1899, phenacetin was popular for many decades, particularly in widely advertised over-the-counter "headache mixtures", usually containing phenacetin, an aminopyrine derivative of aspirin, caffeine, and sometimes a barbiturate. Paracetamol is the active metabolite of phenacetin and acetanilide, both once popular as analgesics and antipyretics in their own right. However, unlike phenacetin, acetanilide and their combinations, paracetamol is not considered carcinogenic at therapeutic doses. Von Mering's claims remained essentially unchallenged for half a century, until two teams of researchers from the United States analyzed the metabolism of acetanilide and paracetamol. In 1947 David Lester and Leon Greenberg found strong evidence that paracetamol was a major metabolite of acetanilide in human blood, and in a subsequent study they reported that large doses of paracetamol given to albino rats did not cause methemoglobinemia. In three papers published in the September 1948 issue of the Journal of Pharmacology and Experimental Therapeutics, Bernard Brodie, Julius Axelrod and Frederick Flinn confirmed using more specific methods that paracetamol was the major metabolite of acetanilide in human blood, and established that it was just as efficacious an analgesic as its precursor. They also suggested that methemoglobinemia is produced in humans mainly by another metabolite, phenylhydroxylamine. A follow-up paper by Brodie and Axelrod in 1949 established that phenacetin was also metabolised to paracetamol. This led to a "rediscovery" of paracetamol. It has been suggested that contamination of paracetamol with 4-aminophenol, the substance von Mering synthesised it from, may be the cause for his spurious findings. Paracetamol was first marketed in the United States in 1950 under the name Triagesic, a combination of paracetamol, aspirin, and caffeine. Reports in 1951 of three users stricken with the blood disease agranulocytosis led to its removal from the marketplace, and it took several years until it became clear that the disease was unconnected. Paracetamol was marketed in 1953 by Sterling-Winthrop Co. as Panadol, available only by prescription, and promoted as preferable to aspirin since it was safe for children and people with ulcers. In 1955, paracetamol was marketed as Children's Tylenol Elixir by McNeil Laboratories. In 1956, 500 mg tablets of paracetamol went on sale in the United Kingdom under the trade name Panadol, produced by Frederick Stearns & Co, a subsidiary of Sterling Drug Inc. In 1963, paracetamol was added to the British Pharmacopoeia, and has gained popularity since then as an analgesic agent with few side-effects and little interaction with other pharmaceutical agents. Concerns about paracetamol's safety delayed its widespread acceptance until the 1970s, but in the 1980s paracetamol sales exceeded those of aspirin in many countries, including the United Kingdom. This was accompanied by the commercial demise of phenacetin, blamed as the cause of analgesic nephropathy and hematological toxicity. In 1988 Sterling Winthrop was acquired by Eastman Kodak which sold the over the counter drug rights to SmithKline Beecham in 1994. Available without a prescription since 1959, it has since become a common household drug. Patents on paracetamol have long expired, and generic versions of the drug are widely available.
Analgesic and Paracetamol · Ibuprofen and Paracetamol ·
Patent ductus arteriosus
Patent ductus arteriosus (PDA) is a condition wherein the ductus arteriosus fails to close after birth.
Analgesic and Patent ductus arteriosus · Ibuprofen and Patent ductus arteriosus ·
Renal colic
Renal colic is a type of abdominal pain commonly caused by kidney stones.
Analgesic and Renal colic · Ibuprofen and Renal colic ·
Rheumatoid arthritis
Rheumatoid arthritis (RA) is a long-term autoimmune disorder that primarily affects joints.
Analgesic and Rheumatoid arthritis · Ibuprofen and Rheumatoid arthritis ·
Stevens–Johnson syndrome
Stevens–Johnson syndrome (SJS) is a type of severe skin reaction.
Analgesic and Stevens–Johnson syndrome · Ibuprofen and Stevens–Johnson syndrome ·
Stroke
A stroke is a medical condition in which poor blood flow to the brain results in cell death.
Analgesic and Stroke · Ibuprofen and Stroke ·
Toxic epidermal necrolysis
Toxic epidermal necrolysis (TEN) is a type of severe skin reaction.
Analgesic and Toxic epidermal necrolysis · Ibuprofen and Toxic epidermal necrolysis ·
Vomiting
Vomiting, also known as emesis, puking, barfing, throwing up, among other terms, is the involuntary, forceful expulsion of the contents of one's stomach through the mouth and sometimes the nose.
The list above answers the following questions
- What Analgesic and Ibuprofen have in common
- What are the similarities between Analgesic and Ibuprofen
Analgesic and Ibuprofen Comparison
Analgesic has 283 relations, while Ibuprofen has 151. As they have in common 36, the Jaccard index is 8.29% = 36 / (283 + 151).
References
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