1) BENZYL PENICILLIN - prophylaxis (Benzathine)/meningitis

Procaine; I.M. w/ Comb P.G; I.V. & I.M.., Benzathine; I.M. , Penicillin V; oral + Phenethicillin

2) Resistant Penicillin - one indication - Anti-Staph

Methicillin, Cloxacillin, Dicloxacillin, Flucloxacillin, Nafcillin - Methoxanaf

3) Amino-Penicillins - Broad -SPECTRUM PENICILLINS

Amoxicillin & Ampicillin; Pros Piva, Tala, Paca

4) Anti-Pseudomonal Penicillins pseudmonas & ampicillin resistant proteus

Carbencillin, Ticarcillin, Azlocillin, Mezlocillin, and Piperacillin cillins exception Methoxanaf

5) Amidino-Penicillens

Mecillinam, Pivmecillinam. Nam

(Penicillen_ G)Penicillenase resistant (Anti-staph).- Amino penicillins (Broad Spectrum)- Anti-Pseudomonal
Spectrum- Gram +ve: Streptococci Pneumococci Staphylcocci Gram –ve: Gonorrhea Treponema- Staphylcocci Only- Pen G like **G-**ve: Salmonella Shigella Proteus H.Influenza
- +

- pseudomonas and

- anerobes.
Beta Lactamase susceptibility- Yes- No- Yes- Yes
Can Be combined with Clavulanic Acid to make it resistant (Hepatotoxic)

PENICILLIN/BETA-LACTAMASE INHIBITOR

COMBINATIONS Agents: synergism effect to oppose bacterial resistance

-The beta-lactamase inhibitors (sulbactam, clavulanate, avibactam and tazobactam) counter beta-lactamases; these drugs mimic the structure of beta-lactams but have little antimicrobial activity on their own. They bind to beta-lactamases irreversibly, preventing the beta-lactamase from destroying any beta-lactams that are coadministered and enabling the therapeutic beta-lactam to be effective.

  • Clavulinic acid (hepatotoxic) has little antibacterial activity but inhibit the activity of B-lactamase enzyme by competitive inhibition. This combined with amoxycillin (Augmentin) , this extends the spectrum of amoxycillin  to include B-lactamase producing organisms. Other B-lactamase inhibitors include sulbactam, which can combine with ampicillin to extend its spectrum (Unasyn).**

  • N.B: New beta-lactamases with the ability to destroy many types of beta lactams are continually being discovered and are becoming more prevalent.

When considering the activity of a beta-lactamase inhibitor combination, remember that the beta-lactamase inhibitor only frees up the beta-lactam to kill the organism—it doesn’t enhance the activity. Therefore, the combination products are active only against the bacteria that the beta-lactam in the combination has intrinsic activity against in the absence of beta-lactamase production. For example, ampicillin/sulbactam is active against beta-lactamase producing E coli because ampicillin alone is active against non-beta-lactamase producing E coli. However, it has no useful activity against P aeruginosa, because ampicillin lacks activity against this organism.

  • In contrast, piperacillin/tazobactam is active against P aeruginosa because piperacillin itself is active. Though these drugs have very broad spectra of activity, there are differences among the agents. Keep in mind the rule that beta-lactamase inhibitors restore activity, not add to it, to set them straight.

  • Empiric therapy with piperacillin/tazobactam. Because they have activity against aerobes and anaerobes, they are a good empiric choice for mixed infections, such as intra-abdominal infections, diabetic ulcers, and aspiration pneumonia.

  • Amoxicillin/clavulanate is used for upper and lower respiratory tract infections when beta-lactamase–producing organisms are found or suspected. It can also be useful for UTIs when resistance to other drugs is seen.