For anyone struggling with his math... 70% of 300mg is 210mg entering hepatic portal system with the remaining 90mg being excreted through feces 60% of that 210mg entering the liver is deactivated by the liver resulting in 126mg of the drug being inactivated. 210mg - 126mg = 84mg or 28% of initial dose entering systemic circulation with its bioavailability intact. Hope that helps.
@gelaiiyke86893 жыл бұрын
Yes! Thank you so much
@Letsgetdancing_3 жыл бұрын
Thanks a lot
@44-burhanuddin892 жыл бұрын
My methodology is also this
@stranger.97 Жыл бұрын
Thanks
@ayisha1943 Жыл бұрын
Hello! I didn't understand one thing why would we subtract 60% from 100% when 70% drug reaches the portal system and 30% already removed from faeces even before reaching portal??
@vikas-li3hf Жыл бұрын
Sir im vikas kumar from India in Lucknow city You so esaly study i understood little You are teaching good God bless you
@braid95482 жыл бұрын
this is a great video!! you explain First pass so clearly!! Its a shame i can't reference a youtube video for my assignment :(
@xtinesssss2 жыл бұрын
Can you explain in your last question how it would be higher? I thought when taken orally it causes a lower effect because not everything is metabolized as opposed to parenteral route where it has a higher effect because it goes straight to circulatory. Can you explain that part?
@Dr_ahmedfouad2 жыл бұрын
It would be lower because first pass effect, that’s why the availability of IV is %100. The answer is wrong
@areejahmed91882 жыл бұрын
He is asking about the dose that should be taken orally to give the same effect that IV route give so you need to make the dose higher because of the first pass effect (not asking if the effect would be higher or lower)
@Dr_ahmedfouad2 жыл бұрын
@@areejahmed9188 صحيح عاشت ايدج ✅
@werdsdanoliees78712 жыл бұрын
Dosage
@jameswhitaker4357 Жыл бұрын
Not a med student but love to do health studying. This explains a lot very effectively. Thank you sir! I’m in the Data Science field so the math was refreshingly simple. It’s more of understanding processes, eh? Orally our drugs will never be 100% bioavailable.
@physiopathopharmaco4190 Жыл бұрын
Awesome James - love your curiosity for learning!
@jameswhitaker4357 Жыл бұрын
@@physiopathopharmaco4190 it helps a lot, when explaining to my grandmother why she should seek foods that are bioavailable in b12 vs the vitamin form. And the fiber benefit and w/e. My curiosity comes from taking the right amount of vitamins + eating foods with high bioavailability of those vitamins we need. 🙂
@Bmarker2993 жыл бұрын
Excellent! Well done. Gifted teacher. Beautiful voice
@physiopathopharmaco41902 жыл бұрын
Wow, thank you!
@dianawilliams68693 жыл бұрын
You should do like a voiceover for a video game (like a walkthrough) unrelated but I think it would work together
@danielclarke2577 Жыл бұрын
amazing made a complex subject easier and the 2 questions at the end really helped
@suryaprasantnaram51412 жыл бұрын
Its an awesome explanation through how drug works in the body
@eubutuoy6 ай бұрын
Is there a database that lists chemicals and information about first-pass metabolism?
@syedaamerahussaini89253 жыл бұрын
Thank you sir! It is very helpful! Got the concept really quickly!
@physiopathopharmaco41903 жыл бұрын
That’s great thanks
@complex58134 ай бұрын
-First pass metabolism is the broken down action of the liver. -Bioavailability is a percentage
@장보윤-q9v Жыл бұрын
Very clear and understandable even for non-english speaker! Thanks!!! :)
@tiki4045 Жыл бұрын
Thank you! Awesome breakdown.
@bitchimee29524 жыл бұрын
hey, please why would you subtract 60% from 100 if 30% was already removed through faeces. shouldn't it be 60% subtracted from what got into the liver which is 70% ?
@physiopathopharmaco41904 жыл бұрын
You would multiply 70% by 40% since these were the %s that moved on at the 2 points they could have been taken out.
@ralphsmith26832 жыл бұрын
YOU are CORRECT and HE is NOT
@otterley_30415 жыл бұрын
THANK YOU SO MUCH,. You are a godsend!
@physiopathopharmaco41905 жыл бұрын
That’s very generous, thank you
@raoarslan37542 жыл бұрын
This help me alot and got complete Concept about this But I dont Understand the Last Question only.
@ayadwidar8824 Жыл бұрын
It was simple and useful thank you so much ❤
@clarity82965 жыл бұрын
Love the content. What do you use to create your videos?
@zamanmakan27293 жыл бұрын
Thanks a lot! I'm wondering if first pass is part of phase 1 or do first pass and phase 1 happen at the same time for prodrugs? Thanks a lot
@BaoTran-ls7oy Жыл бұрын
Thank you for this video!
@physiopathopharmaco4190 Жыл бұрын
You are so welcome!
@Jiha-ed9lv7 ай бұрын
Thank you sooo much. Very helpful!,,
@physiopathopharmaco41907 ай бұрын
Glad it was helpful!
@michaelavillanueva2034 жыл бұрын
Thanks man, helped me understand my lesson
@shashidutt50122 жыл бұрын
You are an excellent teacher!
@aliayad59672 жыл бұрын
Shouldn't the answer be B because of first pass effect ??!
@physiopathopharmaco41902 жыл бұрын
Remember that intravenous bypasses the 1st pass effect, if you are changing to oral, now you have 1st pass effect so to compensate you must increase the dose
@aliayad59672 жыл бұрын
Ohh, i must misunderstood the question thanx for for explaining it's been a great helpful
@yeshuasage3724 Жыл бұрын
@@aliayad5967 misunderstanding the question costs many pharma students Its almost an english test as well as a pharma test Always read the q many times over and good luck
@trickstertrip596210 ай бұрын
Got me too 😅😅😅
@truebeliever64374 жыл бұрын
do IV, intradermal, rectal drugs get metabolized by the liver?
@physiopathopharmaco41904 жыл бұрын
Yes but not on the first pass
@truebeliever64374 жыл бұрын
wow quick reply thanks
@Prfinity8 ай бұрын
Useful concepts
@seedsofhope86434 жыл бұрын
OMG! Thank u so much, such an amazing video :)
@kabiswaaugustine726424 күн бұрын
The answer is A because first pass effect reduces the bioavailability of the drug thus we need to administer a higher dose to
@katherinec83963 жыл бұрын
This is a awesome explanation!
@ralphsmith26832 жыл бұрын
AN awesome...NOT a awesome
@idilmohamed_5 жыл бұрын
This helped a lot! THANK YOU.
@physiopathopharmaco41905 жыл бұрын
Awesome- you’re very welcome 😊
@CilmiFaafiye3 жыл бұрын
Idil maxamed adiga ila somali ah ee seetahay wll ? hhhhhh mar arday medicine ah bad tahay wll ?
@pingmacalos5002 жыл бұрын
sir thank you very much for this!!!
@zopilote_40004 жыл бұрын
can first pass metabolism vary? like can i take a medication and one time it gets absorbed a lot and then the next not as much? can it vary based on food consumption or other factors? is it different in different people? or is it constant for a drug?
@dr.sohataher94134 жыл бұрын
Ofcourse it vary with food.. See omeprazole and sulfur containing drug..
@medicalscience15282 жыл бұрын
Good Question !
@tubamalik92322 жыл бұрын
good explaining
@adamstevens55184 жыл бұрын
The thing I don't understand is, I see sources that say 50% of stomach contents empty in 2.5 to 3 hours, yet oral drugs can take affect in less than an hour in some cases. If most of the drug doesn't get emptied from the stomach for hours, how does it take affect so fast? It goes directly from the stomach to the bloodstream?
@stephanieosmond50592 жыл бұрын
My understanding would be that because the drug that doesn't get emptied is then going to systemic circulation whereas the drug that has been moved onto to be emptied has one been modified or broken down then does it have to travel through the rest of the GI system?
@truebeliever64374 жыл бұрын
which is better for a patient with cirrhosis to receive? IV Tylenol or IV Fentanyl and IV Hydromorphone?
@physiopathopharmaco41904 жыл бұрын
Hepat Mon. 2014 Oct; 14(10): e23539. Published online 2014 Oct 11. doi: 10.5812/hepatmon.23539 PMCID: PMC4250965 PMID: 25477978. “Because of its proven safety profile (when given in recommended doses) and the lack of sedative effects and absence of nephrotoxicity, acetaminophen is the preferred analgesic in patients with liver disease including cirrhosis. However, because acetaminophen overdose is known as one of the most common cause of liver failure, it is not surprising that the majority of pain practitioners are not willing to prescribe it to patients with any form of liver disease.”
@rehamgamal32853 жыл бұрын
Nicely subscribed.
@gladysma3088 ай бұрын
2:06 Bioavailability
@dalilaalves39382 жыл бұрын
Very well explained! Cheers 😉
@vikas-li3hf Жыл бұрын
Hiii i am vikas from India
@SanjeevKumar-lt1wc4 жыл бұрын
Thanks very much
@bhuvaneshwariravichandran82022 жыл бұрын
Please explain that why we should subtract 60% from 100% not from 70% which is the percentage of drug that gets into the liver as the 30% of drug is already being excreted into feces
@sullypwz78642 жыл бұрын
how do drugs flow to hepatic arteries? i thought blood only flow from artery to cappilaries not opposite.
@xixi26934 жыл бұрын
Sir please I have a question When everything exists within nature, whether it is vegetable fruits or allopathic medicine, how the body detects that allopathic medicine is a foreign material ? ? Because allopathic medicine is man made but it from a combination of the matter that exists within the nature so we consider it as natural. Then how the body detects that allopathic is foreign material ?
@karthiksadanand33504 жыл бұрын
Though I'm far from an expert in this field, I assume anything foreign that the body encounters (after being ingested) will be absorbed and then passed through the liver. After all, vegetables and fruits are just made of organic matter that can then be broken down. This will then be absorbed into the bloodstream and can the be passed through the liver (for metabolism). This is an evolutionary mechanism I believe to make sure that the chance of any foreign molecules causing harm to humans is drastically minimised.
@kasunrodrigo65922 жыл бұрын
Very correct as per my understanding. Alcohol is a great example of such a mechanism very interesting to understand if you could dig deeper
@passntesam33468 ай бұрын
❤❤❤❤
@aliaelfaham61313 жыл бұрын
Thank you very much 🌼
@dorianken14874 жыл бұрын
you're amazing, thank you!
@medicalscience15282 жыл бұрын
So in simple words , we can say that liver eliminate 'extra drugs' and keep only that amount in body which is needed ? Please help clear the concept.
@zizojaezekeom35654 ай бұрын
No we can't say that because the liver isn't conscious about what it's doing, it doesn't know what's the important amount you need
@medicalscience15284 ай бұрын
@@zizojaezekeom3565 Ok. Thanks. Then how this mechanism work ? Can u tell if u know
@ruththompson52803 жыл бұрын
Good stuff
@mycenaeangal93124 жыл бұрын
Does this scale linearly with dosage?
@amawor54045 жыл бұрын
thank you god bless u
@pramudimekala29594 жыл бұрын
Thank u so much, that is so helpful😊
@doctorbase23643 жыл бұрын
Super amazing
@lanyafalah20283 жыл бұрын
Thank you so much 🥰
@Dr.BelloAliyu4 жыл бұрын
What's the main difference between Bioavailability and Biotransformation because I'm totally confused sir.
@physiopathopharmaco41904 жыл бұрын
Biotransformation is just altering of a drug by the body. Bioavailability is the percentage of the drug that makes it to systemic circulation.
@Dr.BelloAliyu4 жыл бұрын
@@physiopathopharmaco4190 thanks u very much sir.. really appreciate
@christin55694 жыл бұрын
GOD'S Bless you...good
@muygechlim65864 жыл бұрын
Really helpful. Thank you 🙏
@physiopathopharmaco41904 жыл бұрын
So glad!
@juliabl64715 жыл бұрын
how is first pass metabolism or first pass effect different to the concept of enterohepatic circulation?
@physiopathopharmaco41905 жыл бұрын
First pass is breakdown of the drug by the liver before it reaches systemic. Enterohepatic circulation is circulation from the gut to the portal circulation to the liver back into the bile and back into the small intestine - so its circulating from the gut to the hepatic and back to the gut and back to the hepatic in a circular pattern - so much less of it reaches systemic circulation.
@juliabl64715 жыл бұрын
@@physiopathopharmaco4190 thank you so much!! Very helpful!
@Mariam-nv1fk5 жыл бұрын
Nice but didn't understand the last qs ?👍🏻
@Dravyaguna5 жыл бұрын
First pass effect causes lower amount of drug available for final action hence while shifting from IV to oral we have to increase the dose.
@otpifree5 жыл бұрын
That you have to INCREASE the amount of drug given PO vs the original amount given via IV to account of the big loss due to first pass
@CenobiteBeldar5 жыл бұрын
@@otpifree I might be wrong, but I'm guessing that if we were to give a high first-pass effect IV, it'd be considered over dose?
@CenobiteBeldar5 жыл бұрын
@Montgomery Young So, it depends on how you administer it then. Just because it's IV, doesn't mean it's overdose.
@suparnadhara58363 жыл бұрын
Thanks sir
@taiwovictoria15873 жыл бұрын
Thank you!!
@sayan22034 жыл бұрын
the questions were good
@diborazeleke5288 Жыл бұрын
Very nice🥰
@lajasadi94065 жыл бұрын
thank you so helpful
@Jacqueline84 жыл бұрын
YOU saved me :)
@nizamudin55m124 жыл бұрын
hi
@deepakrawat_28vcsg784 жыл бұрын
Ty
@sokinahnasser60654 жыл бұрын
AMAZING 🔥🔥🔥💯
@797brm5 жыл бұрын
Great content!
@zinenazm1641 Жыл бұрын
Why the answer of the questions doesn't b??
@مرتضىنعمههادي5 жыл бұрын
So so so nice
@physiopathopharmaco41905 жыл бұрын
Thank you for the comment
@clarity82965 жыл бұрын
@@physiopathopharmaco4190 What do you use to draw you videos?
@HEEM_SLEEPY3 жыл бұрын
Thanks :)
@roronoazoro32042 жыл бұрын
This video is so damn helpful
@empty2thecore Жыл бұрын
not me jumping around because i solved an equation that is taught in 8th grade
@wraithdefilerjj10393 жыл бұрын
The last question in the video, isn't the answer gonna be IV?
@physiopathopharmaco41903 жыл бұрын
The oral dose would have to be higher to compensate for the first pass effect.
@ivynya293 жыл бұрын
@@physiopathopharmaco4190 thanks. I missed the last part of the question too. I thought is was what should you expect as it pertains to the bioavailability. Yes, the oral dose will need to be higher in order to deliver the same effect as IV. But then depending on the drug the possibility of that will need to consider other parameters.
@MsServando5 жыл бұрын
Why would the answer be "A"?
@physiopathopharmaco41905 жыл бұрын
You would have to give a higher oral dose because a portion of that oral dose will be removed by the liver before it makes it to systemic circulation.
@MsServando5 жыл бұрын
Ohhhh, thank you so much...I completely misread the question
@Sesinam287511 ай бұрын
I don't understand the question
@DD-kc9lu Жыл бұрын
Is this pedro pascal speaking?
@ritlavkriraj9025 Жыл бұрын
How A is correct
@Medicotopics3 жыл бұрын
Editer name !
@SaadSaad-mb4py4 жыл бұрын
Fantastic
@olha_2 жыл бұрын
As for the question at the end, depends on how intelligent your doctor is
@JIMMYJREVIEWS_thaiM-A-F-I-A Жыл бұрын
Can anyone help me with just 20 mg ? PLEASE!!!!
@A_friend-pr6ji Жыл бұрын
Hi, in this case, you should multiply 20*0,7*0,4, resulting in 5,6mg. Here the explanation: 70% of the drug reaches the liver (20*0,7 = 14mg, and 6mg are lost) From the 14mg that are in the liver, 40% goes into the bloodstream (14*0,4 = 5,6mg), and 8,4mg are lost (14*0,6 = 8,4). I hope this helps you.
@Dravyaguna5 жыл бұрын
Nicely described
@physiopathopharmaco41905 жыл бұрын
🙏
@arshusvlog97204 жыл бұрын
@@physiopathopharmaco4190 i have a doubt sir. What about Acetamonophen / paracetamol ? As iv we give 1g but while change to oral we give only 650mg. Why?
@arshusvlog97204 жыл бұрын
@@physiopathopharmaco4190 also regarding CEFUROXIME. we give iv as 1.5g. But while switching to oral we prescribe 500mg only.. !!! Why sir?