| | | C<sub>16</sub>H<sub>15</sub>N<sub>5</sub>O<sub>7</sub>S<sub>2</sub> | | | | | | <img src="../IMAGES/pet.gif"/> | Suprax, Trixon-O, Taxone-O. | This substance is a second-generation cephalosporin antibiotic. It is a broad spectrum cephalosporin antibiotic and is commonly used to treat bacterial infections of the ear, urinary tract and upper respiratory tract. | | | | <a href="PDF/P_InfoEn/C-054.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/C-054.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/C-054.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/C-054.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/CAD-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/CAD-1000.pdf" Target="_blank">Previous Year</a> | |
| | | C<sub>16</sub>H<sub>19</sub>N<sub>3</sub>O<sub>5</sub>S | | | | | | <img src="../IMAGES/pet.gif"/> | [2S-[2alpha,5alpha,6beta(S*)]]-6-[[2-amino-2-(4-hydroxyphenyl) acetyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid; p-Hydroxyampicillin; 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-(2-amino-2-(p-hydroxyphenyl)acetamido)-3,3-dimethyl-7-oxo, D-; 6-; (-)-6-[2-amino-2-(p-hydroxyphenyl)acetamido]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid; 6-(p-Hydroxy-alpha-aminophenylacetamido) pencillanic acid; 6-(p-hydroxy-alpha-aminophenylacetamido)penicillanic acid; 6-(D-(-)-p-Hydroxy-alpha-aminobenzyl)penicillin; 6-[D(-)-alpha-amino-p-hydroxyphenylacetamido]penicillanic acid; alpha-amino-p-hydroxybenzyl penicillin; Alphacin; Agram (Trihydrate); Alfamox; Almodan; Amocilline; Amoclen; Amodex (Trihydrate); Amolin; Amopen; Amopenixin; Alphamox; Amoxi; Amoxidin (Trihydrate); Amoxibiotic (Trihydrate); Amoxicilline; Amoxicillin trihydrate; Amoxidal (Trihydrate); Amoxil; Amoxil (Trihydrate); Amoxillat (Trihydrate); Amoxipen; Amoxi-Wolff (Trihydrate); Amoxycillin; Amoxypen (Trihydrate); AMPC; Anemolin; Aspenil; Augmentin; Betamox; Bristamox; Cabermox; Cemoxin; Cilamox; Clamoxyl; Clamoxyl (Trihydrate); Cuxacillin; D-(-)-alpha-amino-p-hydroxybenzyl penicillin trihydrate; Delacillin; Efpenix; Fisamox; Grinsil; Histocillin; Ibiamox; Imacillin; Larotid; Moxacin; Optium; Ospamox; Piramox; Polymox; Sawacillin; Sawacillin (Trihydrate); Simoxil; Sumox; Trimox; Trimox (Trihydrate); Utimox; Wymox (Trihydrate); | Amoxicillin or amoxycillin is a moderate-spectrum beta-lactam antibiotic
used to treat bacterial infections caused by susceptible microorganisms.
It is usually the drug of choice within the class because it is better absorbed,
following oral administration, than other beta-lactam antibiotics.
Amoxicillin is susceptible to degradation by beta-lactamase-producing
bacteria, and so may be given with clavulanic acid to decrease its susceptibility.
It was developed by Beecham in 1972 and is currently marketed by
GlaxoSmithKline (the inheritor company) under the original trade name
Amoxil. | | | | <a href="PDF/P_InfoEn/A-030.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/A-030.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/A-030.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/A-030.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/CAD-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/CAD-1000.pdf" Target="_blank">Previous Year</a> | |
| | | | Dicloxacillin sodium salt hydrate | | | | | <img src="../IMAGES/pet.gif"/> | | Dicloxacillin is a narrow spectrum beta-lactam antibiotic of the penicillin
class. It is used to treat infections caused by susceptible Gram-positive
bacteria. Notably, it is active against beta-lactamase-producing organisms
such as Staphylococcus aureus, which would otherwise be resistant to
most penicillins. It is very similar to flucloxacillin and these two agents are considered interchangeable. Dicloxacillin is available under a variety
of trade names. | | | | <a href="PDF/P_InfoEn/D-058.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/D-058.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/D-058.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/D-058.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/CAD-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/CAD-1000.pdf" Target="_blank">Previous Year</a> | |
| | | C<sub>16</sub>H<sub>16</sub>N<sub>5</sub>NaO<sub>7</sub>S<sub>2</sub> | | | | | | <img src="../IMAGES/pet.gif"/> | Claforan; Cefotaxime sodium; sodium salt of 7-[2-(2-amino-4-thiazolyl)glyoxylamido]-3-(hydroxymethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate 7 (Z)-(O-methyloxime), acetate (ester); | A cephalosporin that belongs to a group of broad-spectrum antibiotic
derived from species of fungi of the genus Cephalosporium and are related
to the penicillins in both structure and mode of action but relatively
penicillinase-resistant antibiotics. Third-generation cephalosporins are
more active against gram-negative organisms but less active against grampositive
organisms than second-generation agents; examples are cefoperazone,
cefotaxime, ceftriaxone, ceftazidime, ceftizoxime, and moxalactam. | | | | <a href="PDF/P_InfoEn/C-040.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/C-040.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/C-040.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/C-040.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/CAD-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/CAD-1000.pdf" Target="_blank">Previous Year</a> | |
| | | C<sub>22</sub>H<sub>24</sub>N<sub>2</sub>O<sub>8</sub>.H<sub>2</sub>O | | | | | | <img src="../IMAGES/pet.gif"/> | | Doxycycline is a semisynthetic broad-spectrum antibiotic or antibacterial and
belongs to the tetracycline family. It is used to treat urinary tract infections,
gum disease, and bacterial infections such as gonorrhea, chlamydia
and Bacillus anthracis. It is also used to treat acne. | | | | <a href="PDF/P_InfoEn/D-059.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/D-059.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/D-059.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/D-059.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/CAD-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/CAD-1000.pdf" Target="_blank">Previous Year</a> | |
| | | C<sub>21</sub>H<sub>27</sub>N<sub>5</sub>O<sub>9</sub>S<sub>2</sub> | | | | | | <img src="../IMAGES/pet.gif"/> | | This substance is an oral, third-generation cephalosporin antibiotic. It is active against most Gram-positive and Gram-negative organisms. It is commonly used to treat acute otitis media, pharyngitis, sinusitis, and gonorrhea. Veterinary uses is also found. | | | | <a href="PDF/P_InfoEn/C-055.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/C-055.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/C-055.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/C-055.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/CAD-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/CAD-1000.pdf" Target="_blank">Previous Year</a> | |
| | | C<sub>37</sub>H<sub>67</sub>NO<sub>13</sub> | | | | | | <img src="../IMAGES/pet.gif"/> | Abomacetin; Ak-Mycin; Aknin; Drmysin; E-Base; E.E.S; Emgel; EMU; E-mycin; Ergel; Eritocina; Eritrocina; Erthrogran; Eryacne; ERYC; Erycen; Erycette; Erycin; Erycinum; Ery Derm; Erymax; Erypar; ERY-PED; ERY-TAB; Erythro; Erythrocin; Erythroguent; Erythromast; Erythromast 36; Erythromid; Erythromycin; Gallimycin; Ilocap; Ilosone; Ilotycin; Inderm; L-alpha-Egg-phosphatidylcholine; P.C.E.; Pediamycin; Retcin; Robimycin; Statcin; Staticin; Stiemycin; Torlamicina; Torlamicna; T-Stat; USP; Wintrocin; Wyamycin-s; | Erythromycin is a macrolide antibiotic that has an antimicrobial spectrum
similar to or slightly wider than that of penicillin, and is often used for
people that have an allergy to penicillins. For respiratory tract infections,
it has better coverage of atypical organisms, including mycoplasma and
Legionellosis. It is also used to treat outbreaks of chlamydia, syphilis,
acne, and gonorrhea. In structure, this macrocyclic compound contains
a 14-membered lactone ring with ten asymmetric centers and two sugars
(L-cladinose and D-desoamine), making it a compound very difficult to
produce via synthetic methods. Erythromycin is produced from a strain
of the actinomycete Saccharopolyspora erythraea, formerly known as
Streptomyces erythraeus. | | | | <a href="PDF/P_InfoEn/E-024.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/E-024.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/E-024.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/E-024.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/CAD-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/CAD-1000.pdf" Target="_blank">Previous Year</a> | |
| | | C<sub>43</sub>H<sub>74</sub>N<sub>2</sub>O<sub>14</sub> | | | | | | <img src="../IMAGES/pet.gif"/> | Foromacidin; Leucomycin; Provamycin; Rovamicina; Rovamycin; Selectomycin; Sequamycin; Spiramycin; | Spiramycin is a macrolide antibiotic. It is used to treat toxoplasmosis.
Although routinely used in Europe, spiramycin is still considered an
experimental drug in the United States. Used in Europe since 2000 year as â€Rovamycineâ€, produced by Rhone-Poulenc Rorer, France and Eczacibasi Ilae, Turkey. | | | | <a href="PDF/P_InfoEn/S-012.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/S-012.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/S-012.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/S-012.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/CAD-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/CAD-1000.pdf" Target="_blank">Previous Year</a> | |
| | | C<sub>38</sub>H<sub>69</sub>NO<sub>13</sub> | | | | | | <img src="../IMAGES/pet.gif"/> | 6-O-methylerythromycin; 6-0-methylerythromycin; A-56268; Biaxin; Clarithromycin; Clathromycin; Klacid; TE-031; | Clarithromycin, 6-0-methylerythromycin, belonging to the macrolide
group, has a close structural and biological similarity with erythromycin.
It is effective against a broad spectrum of gram-positive and gram-negative
bacteria. It is used to treat respiratory tract infections and soft tissue infections.
It is used to treat duodenal ulcer associated with Helicobacter pylori
infections in combination with omeprazole. | | | | <a href="PDF/P_InfoEn/C-041.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/C-041.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/C-041.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/C-041.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/CAD-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/CAD-1000.pdf" Target="_blank">Previous Year</a> | |
| | | C<sub>8</sub>H<sub>8</sub>NO<sub>5</sub>K | | | | | | <img src="../IMAGES/pet.gif"/> | | This chemical is a drug which is given with antibiotics. While not effective by itself as an antibiotic, when combined with penicillin-group antibiotics, it can overcome antibiotic resistance in bacteria that secrete β-lactamase, which otherwise inactivates most penicillin’s.
In its most common form, the potassium salt potassium clavulanate is combined with:
Amoxicillin (co-amoxiclav, trade names: Augmentin, Tyclav (Beximco), and others) or
Ticarcillin (co-ticarclav, trade name Timentin).<br/><b>Doctor information:</b><br/>
This product contains 10% microcrystalline cellulose. | | | | <a href="PDF/P_InfoEn/P-040.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/P-040.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/P-040.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/P-040.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/CAD-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/CAD-1000.pdf" Target="_blank">Previous Year</a> | |
| | | | | | | | | <img src="../IMAGES/pet.gif"/> | | Co-trimoxazole is an antibiotic combination of trimethoprim and sulfamethoxazole,
in the ratio of 1 to 5, used in the treatment of a variety of
bacterial infections. The name co-trimoxazole is the British Approved
Name, and has been marketed worldwide under many trade names including
Septrin (GSK), Bactrim (Roche), and various generic preparations.
According to the American Hospital Formulary Service, “co-trimoxazole usually is bactericidal.†Other sources list this antibiotic as bacteriostatic. | | | | <a href="PDF/P_InfoEn/C-042.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/C-042.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/C-042.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/C-042.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/CAD-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/CAD-1000.pdf" Target="_blank">Previous Year</a> | |
| | | C<sub>16</sub>H<sub>18</sub>FN<sub>3</sub>O<sub>3</sub> | | | | | | <img src="../IMAGES/pet.gif"/> | Norfloxacine; Noroxin; 1-ethyl-6-fluoro-4-oxo-7-piperazin-1-yl-1H-quinoline-3-carboxylic acid. | Norfloxacine is an oral broad-spectrum fluoroquinolone antibacterial agent used in the treatment of urinary tract infections. The mechanism
of action of norfloxacin involves inhibition of the A subunit of bacterial DNA gyrase, an enzyme which is essential for DNA replication. | | | | <a href="PDF/P_InfoEn/N-007.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/N-007.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/N-007.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/N-007.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/CAD-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/CAD-1000.pdf" Target="_blank">Previous Year</a> | |
| | | C<sub>17</sub>H<sub>18</sub>FN<sub>3</sub>O<sub>3</sub>.HCl | Ciprofloxacine hydrochloride | | | | | <img src="../IMAGES/pet.gif"/> | Ciprofloxacin; 1,4-dihydro-1-cyclopropyl-6-fluoro-4-oxo-7-(1-piperazinyl)-3-Quinolinecarboxylic acid. | A quinolone antibiotic drug
used mainly to treat the respiratory infections (pneumoniae, pseudomonas,
influenzae), urinary tract infections, the gastrointestinal surgery, typhoid
fever, gonorrhoea (enterotoxigenic strains of Escherichia coli), and
septicaemia. Ciprofloxacin act by inhibiting the bacterial enzymes DNA
gyrase. Other quinolones include cinoxacin; levofloxacin; nalidixic acid;
norfloxacin; ofloxacin.- | | | | <a href="PDF/P_InfoEn/C-043.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/C-043.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/C-043.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/C-043.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/CAD-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/CAD-1000.pdf" Target="_blank">Previous Year</a> | |
| | | C<sub>15</sub>H<sub>12</sub>N<sub>2</sub>O | | | | | | <img src="../IMAGES/pet.gif"/> | 5-carbamoyl-5H-dibenz[b,f]azepine; 5H-Dibenz[b,f]azepine-5-carboxamide; Carbamazepine; Carbamezapine; Carbazepine; Epitol; Tegertol; Tegretol; Teril; | Carbamazepine (“CBZâ€) is an anticonvulsant and mood stabilizing drug,
used primarily in the treatment of epilepsy and bipolar disorder. It is also
used to treat ADD, ADHD, schizophrenia and trigeminal neuralgia.5Hdibenz[
b,f]azepine-5-carboxamide. | | | | <a href="PDF/P_InfoEn/C-044.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/C-044.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/C-044.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/C-044.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/CAD-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/CAD-1000.pdf" Target="_blank">Previous Year</a> | |
| | | C<sub>3</sub>H<sub>4</sub>N<sub>2</sub>O<sub>2</sub> | | | | | | <img src="../IMAGES/pet.gif"/> | 2,4-Imidazolidinedione; 2,4-Imidazolinedione; Hydantoin; Imidazolidine-2,4-dione; | Hydantoin, also known as glycolyurea, is an imidazole analogue.
Hydantoin and its derivatives are used in the preperation of textile softeners,
lubricants, resins, and agrochemicals. They have bacteriostatic and
bacteriacidal capabilities useful preservatives against bacteria and fungi.
They have antibacterial, antifungal, antiprotozoal, and anthelmintic activity.
They are used in manufacturing pharmaceuticals especially anticonvulsant
drugs such as phenytoin, ethotoin, and methyphenytoin. | | | | <a href="PDF/P_InfoEn/H-027.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/H-027.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/H-027.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/H-027.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/CAD-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/CAD-1000.pdf" Target="_blank">Previous Year</a> | |
| | | C<sub>22</sub>H<sub>26</sub>N<sub>2</sub>O<sub>4</sub>S.HCl | | | | | | <img src="../IMAGES/pet.gif"/> | 1,5-Benzothiazepin-4(5H)one,3-(acetyloxy)-5-(2-(dimethylamino)ethyl)-2,3-dihydro-2-(4-methoxyphenyl)-, monohydrochloride, (+)-cis-; Dilacor XR; Diltiazem hydrochloride; Cardizem; Cardizem CD; Cardizem SR; Cardcal; Coras; | Diltiazem HCl is a member of the group of drugs known as benzothiazepines
, which are a class of calcium channel blockers, used in the treatment
of hypertension, angina pectoris, and some types of arrhythmia. It is a
class 3 anti-anginal drug, and a class IV antidysrhythmic. It incites very
minimal reflex sympathetic changes. Diltiazem HCl is a potent vasodilator,
increasing blood flow and variably decreasing the heart rate via
strong depression of A-V node conduction. Its pharmacolgical activity is
somewhat similar to verapamil. | | | | <a href="PDF/P_InfoEn/D-060.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/D-060.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/D-060.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/D-060.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/CAD-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/CAD-1000.pdf" Target="_blank">Previous Year</a> | |
| | | C<sub>9</sub>H<sub>15</sub>NO<sub>3</sub>S | | | | | | <img src="../IMAGES/pet.gif"/> | 1-((2S)-3-mercapto-2-methylpropionyl)-L-proline; Acenorm; Capoten; Capozide; captopril; (S)-1-(3-Mercapto-2-methyl-1-oxopropyl)-L-proline; (S,S)-1-(D-3-Mercapto-2-methyl-1-oxopropyl)-L-proline; | Captopril is an angiotensin-converting enzyme inhibitor (ACE inhibitor)
used for the treatment of hypertension and some types of congestive heart
failure. Captopril was the first ACE inhibitor developed and was considered
a breakthrough both because of its novel mechanism of action and
also because of the revolutionary development process. Captopril’s main
uses are based on its vasodilatation and inhibition of some renal function
activities. Captopril is commonly marketed by Bristol-Myers Squibb under
the trade name Capoten or Inhibace. | | | | <a href="PDF/P_InfoEn/C-045.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/C-045.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/C-045.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/C-045.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/CAD-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/CAD-1000.pdf" Target="_blank">Previous Year</a> | |
| | | C<sub>9</sub>H<sub>8</sub>O<sub>4</sub> | | | | | | <img src="../IMAGES/pet.gif"/> | 2-Acetoxybenzenecarboxylic acid; 2-acetoxybenzoic acid; Alka-seltzer; Anacin; A.S.A.; a.s.a. empirin; asagran; asatard; Ascoden-30; Ascriptin; aspalon; aspergum; aspirdrops; Aspirin; Aspro; asteric; Bayer; benaspir; bialpirinia; Bufferin; caprin; Chlorpheninaurine; Claradin; colfarit; contrheuma retard; Coricidin; Coricidin D; crystar; Darvon compound; delgesic; dolean ph 8; duramax; ECM; Ecotrin; empirin; endydol; entericin; enterophen; enterosarine; entrophen; Excedrin; extren; Gelprin; globoid; helicon; idragin; Measurin; neuronika; Norgesic; Novid; Nu-seals; Persistin; polopiryna; rhodine; Robaxisal; salacetin; salcetogen; saletin; salicylic acid acetate; Solprin; solpyron; Supac; Triaminicin; Vanquish; XAXA; 2-(Acetyloxy)-Benzoic Acid; O-acetylsalicylic acid; o-Carboxyphenyl Acetate; ac 5230; acenterine; acesal; Aceticyl; acetilsalicilico; acetilum acidulatum; acetisal; acetonyl; acetophen; acetosal; acetosalic acid; acetosalin; Acetoxybenzoic acid; acetylin; acetylsal; Acetylsalicylate; Acetylsalicylic acid; acidum acetylsalicylicum; acimetten; acisal; acylpyrin; | Aspirin®, or acetylsalicylic acid, (acetosal) is a salicylate drug often used
as an analgesic (to relieve minor aches and pains), antipyretic (to reduce
fever), and as an anti-inflammatory. It also has an antiplatelet (â€bloodthinningâ€)
effect and is used in long-term, low doses to prevent heart
attacks and blood clot formation in people at high risk for developing
blood clots. | | | | <a href="PDF/P_InfoEn/A-031.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/A-031.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/A-031.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/A-031.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/CAD-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/CAD-1000.pdf" Target="_blank">Previous Year</a> | |
| | | C<sub>14</sub>H<sub>10</sub>Cl<sub>2</sub>NNaO<sub>2</sub> | | | | | | <img src="../IMAGES/pet.gif"/> | 2-((2,6-dichlorophenyl)amino)benzeneacetic acid, monosodium salt; 2-[(2,6-Dichlorophenyl)amino]benzeneacetic acid sodium salt; diclofenac sodium; | Diclofenac (marketed as Voltaren, Voltarol, Diclon, Dicloflex Difen,
Difene, Cataflam, Pennsaid, Rhumalgan, Modifenac, Abitren, Arthrotec
and Zolterol, with various drug dose combinations) is a non-steroidal
anti-inflammatory drug (NSAID) taken to reduce inflammation and an
analgesic reducing pain in conditions such as in arthritis or acute injury.
It can also be used to reduce menstrual pain, dysmenorrhea. The name is
derived from its chemical name: 2-(2,6-dichloranilino) phenylacetic acid. | | | | <a href="PDF/P_InfoEn/D-061B.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/D-061B.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/D-061B.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/D-061B.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/CAD-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/CAD-1000.pdf" Target="_blank">Previous Year</a> | |
| | | C<sub>16</sub>H<sub>14</sub>O<sub>3</sub> | | | | | | <img src="../IMAGES/pet.gif"/> | 2-(meta-Benzoylphenyl) propionic acid; Alrheumat; Ketoprofen; Orudis; Oruvail; | Ketoprofen, (RS)2-(3-benzoylphenyl)-propionic acid (chemical formula
C16H14O3) is one of the propionic acid class of non-steroidal anti-inflammatory
drug (NSAID) with analgesic and antipyretic effects. It acts by
inhibiting the body’s production of prostaglandin. | | | | <a href="PDF/P_InfoEn/K-002B.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/K-002B.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/K-002B.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/K-002B.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/CAD-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/CAD-1000.pdf" Target="_blank">Previous Year</a> | |
| | | C<sub>15</sub>H<sub>13</sub>N<sub>3</sub>O<sub>4</sub>S | | | | | | <img src="../IMAGES/pet.gif"/> | 2H-1,2-Benzothiazine-3-carboxamide, 4-hydroxy-2-methyl-N-2-pyridinyl-, 1,1-dioxide; Candyl; Feldene; Feldene Gel; Fensaid; Mobilis; Pirox; Piroxicam; | Piroxicam (marketed in the U.S. under the trade name Feldene) is a nonsteroidal
anti-inflammatory drug used to relieve the symptoms of rheumatoid
and osteoarthritis, primary dysmenorrhoea, postoperative pain; and act as an analgesic, especially where there is an inflammatory component.
It is also used in veterinary medicine to treat certain neoplasias expressing
cyclooxygenase (COX) receptors, such as bladder, colon, and prostate
cancers. Other brand names for Piroxicam include â€Brexin,†â€Erazon,â€
â€Feldenâ€, â€Feldoral,†â€Hotemin,†â€Pirox von ct,†â€Proponol,†â€Reumador,â€
â€Veral,†and â€Vurdon.†| | | | <a href="PDF/P_InfoEn/P-033.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/P-033.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/P-033.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/P-033.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/CAD-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/CAD-1000.pdf" Target="_blank">Previous Year</a> | |
| | | C<sub>8</sub>H<sub>9</sub>NO<sub>2</sub> | | | | | | <img src="../IMAGES/pet.gif"/> | | | | | | <a href="PDF/P_InfoEn/A-032.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/A-032.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/A-032.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/A-032.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/CAD-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/CAD-1000.pdf" Target="_blank">Previous Year</a> | |
| | | C<sub>8</sub>H<sub>11</sub>N<sub>5</sub>O<sub>3</sub> | | | | | | <img src="../IMAGES/pet.gif"/> | 2-Amino-1,9-dihydro-9-((2-hydroxyethoxy)methyl)-6H-purin-6-one; 2-amino-1,9-dihydro-9-[2-hydroxyethoxy-methyl]-purin-6-one; 9-((2-hydroxyethoxy)methyl)guanine; Aciclovir; Acycloguanosine; Acyclo-V; acyclovir; BW-248U; Vipral; Virorax; Wellcome-248U; Zovirax; Zyclir; | Aciclovir, chemical name acycloguanosine, is a guanine analogue antiviral
drug, marketed under trade names such as Zovirax and Zovir. One
of the most commonly-used antiviral drugs, it is primarily used for the
treatment of herpes simplex virus infections, as well as in the treatment of
herpes zoster (shingles). | | | | <a href="PDF/P_InfoEn/A-033.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/A-033.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/A-033.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/A-033.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/CAD-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/CAD-1000.pdf" Target="_blank">Previous Year</a> | |
| | | | Hydroxyzine hydrochloride | | | | | <img src="../IMAGES/pet.gif"/> | Anxanil; Atarax; Hydroxyzine dihydrochloride; Rezine; Vistaril; | Hydroxyzine is a first-generation antihistamine, of the piperazine class
that is an H1 receptor antagonist. It is used primarily as an antihistamine
for the treatment of itches and irritations, an antiemetic for the reduction
of nausea, as a weak analgesic by itself and as an opioid potentiator, and
as an anxiolytic for the treatment of anxiety. The drug is available in two
formulations, the pamoate and the dihydrochloride or hydrochloride salts.
Vistaril®, Equipose®, Masmoran®, Paxistil®, and Vistaril Pamoate® are preparations of the pamoate salt whilst Atarax®, Alamon®, Aterax®,
Durrax®, Tran-Q®, Orgatrax®, Quiess®, Vistaril Parenteral®, and
Tranquizine® are hydroxyzine hydrochloride. | | | | <a href="PDF/P_InfoEn/H-028.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/H-028.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/H-028.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/H-028.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/CAD-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/CAD-1000.pdf" Target="_blank">Previous Year</a> | |
| | | C<sub>7</sub>H<sub>8</sub>ClN<sub>3</sub>O<sub>4</sub>S<sub>2</sub> | | | | | | <img src="../IMAGES/pet.gif"/> | 3,4-dihydro-6-chloro-7-sulfamoyl-1,2,4-benzothiadiazine-1,1-dioxide; 3,4-dihydrochlorothiazide; oretic; panurin; panurin dichloride; spironolactone/hydrochlorothiazide; thiaretic; urodiazin; vetidrex; 6-chloro-3,4-dihydro-2H-1,2,4-benzothiadiazine-7-sulfonamide-1,1-dioxide; 6-chloro-3,4-dihydro-7-sulfamoyl-2H-1,2,4-benzothiadiazine-1,1-dioxide; Aldactazide; aquarills; aquarius; dichlorosal; diclotride; chlorosulthiadil; cidrex; esidrex; Esidrix; HCTZ; HCZ; hydril; hydrodiuril; Hydro-chlor; Hydrochlorothiazide; Hydro-D; hydrosaluric; hypothiazide; ivaugan; nefrix; neo-codema; neoflumen. | Hydrochlorothiazide, sometimes abbreviated HCT, HCTZ, or HZT is a
popular diuretic drug that acts by inhibiting the kidneys’ ability to retain water. This reduces the volume of the blood, decreasing blood return to the heart and thus cardiac output and, by other mechanisms, is believed to lower peripheral vascular resistance. Hydrochlorothiazide is sold both as a generic drug and under a large number of brand names, including:
Apo-Hydro, Aquazide H, Dichlotride, Hydrodiuril, HydroSaluric, Microzide, Oretic. | | | | <a href="PDF/P_InfoEn/H-029.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/H-029.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/H-029.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/H-029.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/CAD-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/CAD-1000.pdf" Target="_blank">Previous Year</a> | |
| | | C<sub>18</sub>H<sub>34</sub>ClN<sub>2</sub>O<sub>8</sub>PS | | | | | | <img src="../IMAGES/pet.gif"/> | | Clindamycin (phosphate) is a lincosamide antibiotic used in the treatment
of infections caused by susceptible microorganisms. Clindamycin
(phosphate) is a semisynthetic antibiotic derived from lincomycin by
7(S)-chloro-substitution of the 7(R)-hydroxyl group of the lincomycin.
Clindamycin is marketed under various trade names including Dalacin
(Pfizer), Cleocin (Pfizer), and in a foam as Evoclin (Connetics) and
Duac(Stiefel). Clindamycin (phosphate) is used primarily to treat infections
caused by susceptible anaerobic bacteria. Such infections might
include infections of the respiratory tract, septicemia and peritonitis. In
patients with hypersensitivity to penicillins, clindamycin (phosphate)
may be used to treat infections caused by susceptible aerobic bacteria as
well. It is also used to treat bone infections caused by Staphylococcus
aureus. Topical application of clindamycin phosphate can be used to treat
moderate to severe acne. | | | | <a href="PDF/P_InfoEn/C-046.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/C-046.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/C-046.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/C-046.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/CAD-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/CAD-1000.pdf" Target="_blank">Previous Year</a> | |
| | | C<sub>16</sub>H<sub>19</sub>N<sub>3</sub>O<sub>4</sub>S | | | | | | <img src="../IMAGES/pet.gif"/> | Anspor; cefradine; Cephradine; Velosef; | Cefradine or cephradine is a first generation cephalosporin antibiotic.
Effective against a wide range of gram-positive and a limited range of
gram-negative bacteria. | | | | <a href="PDF/P_InfoEn/C-047.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/C-047.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/C-047.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/C-047.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/CAD-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/CAD-1000.pdf" Target="_blank">Previous Year</a> | |
| | | C<sub>16</sub>H<sub>17</sub>N<sub>3</sub>O<sub>4</sub>S | | | | | | <img src="../IMAGES/pet.gif"/> | 7-(D-alpha-amino-alpha-phenylacetamido)-3-methyl-3-cephem-4-carboxylic acid monohydrate; Cefalexin; Cefanex; Cephalexin; C-Lexin; Ibilex; Keflet; Keflex; Keftab; | Cefalexin or cephalexin is a first-generation cephalosporin antibiotic. It
is an orally-administered agent with a similar antimicrobial spectrum to
the intravenous agents cefalotin and cefazolin. It is commonly marketed
under the trade name Keflex (Lilly) or Sporidex (Ranbaxy). Cefalexin is
used to treat urinary tract infections, respiratory tract infections (including
sinusitis, otitis media, pharyngitis, tonsillitis and pneumonia), skin
and soft tissue infections. Although it is not generally considered firstline
therapy for any indication, it is a useful alternative to penicillins in
patients with penicillin hypersensitivity. There is, however, cross-reactivity
in 10% of patients with hypersensitivity to penicillins and carbapenems. | | | | <a href="PDF/P_InfoEn/C-048.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/C-048.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/C-048.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/C-048.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/CAD-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/CAD-1000.pdf" Target="_blank">Previous Year</a> | |
| | | C<sub>13</sub>H<sub>18</sub>O<sub>2</sub> | | | | | | <img src="../IMAGES/pet.gif"/> | (+)-2-(4-Isobutylphenyl)propionic acid; (+/-)-2-(p-isobutylphenyl)propionic acid; 2-(4-isobutylphenyl)propionic acid; 4-Isobutyl-alpha-methylphenylacetic acid; para-Isobutylhydratropic acid; Actiprofen; Adran; Advil; Amersol; Alpha-Methyl-4-(2-methylpropyl)benzeneacetic acid; Amibufen; Anco; Anflagen; Apo-Ibuprofen; Apsifen; Apsifen-F; Artril 300; Bluton; Brufanic; Brufen; Brufort; Buburone; Butylenin; Cap-Profen; Codral; Dolgirid; Dolgit; Dolocyl; Dolo-dolgit; Ebufac; Epobron; Femadon; Fenbid spansule; Haltran; Ibu-attritin; Ibumetin; Ibuprin; Ibuprocin; Ibuprofen; Ibu-slo; Ibutid; Ifen; Lamidon; Lidifen; Liptan; Medipren; Midol 200; Motrin; Mynosedin; Napacetin; Nobfelon; Nobfen; Nobgen; Novoprofen; Nuprin; Nurofen; Paxofen; Pedia-Profen; Pedia-Proten; Profen; Rafen; Rebugen; Roidenin; Rufen; Tab-Profen; Trendar; | Ibuprofen (from the earlier nomenclature iso-butyl-propanoic-phenolic acid) is a non-steroidal anti-inflammatory drug (NSAID) originally marketed as Nurofen and since under various trademarks, including Act-3, Advil, Brufen, Dorival, Herron Blue, Panafen, Motrin, Nuprin and
Burana (Finland), Ipren or Ibumetin (Denmark and Sweden), Ibuprom
(Poland), IbuHEXAL, Ibusal (Finland), Fenpaed (Ireland), Moment (Italy), Ibux (Norway), Ãbúfen (Iceland), Ibalgin (Czech Republic), Bupuren (South Korea), Neofen (Croatia), Eve (Japan), Nurofen and Advil (Australia). It is used for relief of symptoms of arthritis, primary dysmenorrhoea, fever, and as an analgesic, especially where there is an inflammatory component. Ibuprofen has no antiplatelet (blood-thinning) effect. | | | | <a href="PDF/P_InfoEn/I-010A.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/I-010A.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/I-010A.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/I-010A.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/CAD-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/CAD-1000.pdf" Target="_blank">Previous Year</a> | |
| | | C<sub>9</sub>H<sub>7</sub>Cl<sub>2</sub>N<sub>5</sub> | | | | | | <img src="../IMAGES/pet.gif"/> | Lamictal, Lamotrine, Lamogine | This substance is an anticonvulsant drug used in the treatment of epilepsy and bipolar disorder. It is believed to work in adjunct with other drugs when treating clinical depression. It is used in slow-releasing tablets to prevent episodes of seizures. | | | | <a href="PDF/P_InfoEn/L-009.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/L-009.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/L-009.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/L-009.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/CAD-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/CAD-1000.pdf" Target="_blank">Previous Year</a> | |
| | | C<sub>16</sub>H<sub>15</sub>N<sub>4</sub>NaO<sub>8</sub>S | | | | | | <img src="../IMAGES/pet.gif"/> | | This substance is an enteral second-generation cephalosporin antibiotic, which have been on the market since 1983. It is used to treat pneumonia and other lower respiratory tract (lung) infections; meningitis, gonorrhea, skin, blood, bone, joint and urinary tract infections. Injections of the medicine may also be used before, during, and sometimes for a brief period after surgery. | | | | <a href="PDF/P_InfoEn/C-053.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/C-053.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/C-053.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/C-053.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/CAD-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/CAD-1000.pdf" Target="_blank">Previous Year</a> | |