|
|||
DRUGS & SUPPLEMENTS
|
How is the drug helping you? |
WARNING: THROMBOEMBOLIC EVENTS
FEIBA is an Anti-Inhibitor Coagulant Complex indicated for use in hemophilia A and B patients with inhibitors for:
FEIBA is not indicated for the treatment of bleeding episodes resulting from coagulation factor deficiencies in the absence of inhibitors to Anti-Inhibitor Coagulant Complex or coagulation factor IX.
FEIBA is an Anti-Inhibitor Coagulant Complex indicated for use in hemophilia A and B patients with inhibitors for:
FEIBA is not indicated for the treatment of bleeding episodes resulting from coagulation factor deficiencies in the absence of inhibitors to factor VIII or factor IX. (
For intravenous use after reconstitution only.
For intravenous use after reconstitution only
Type of Bleeding | Dose (unit/kg) | Frequency/Duration |
Control and Prevention of Bleeding | 50 - 100 | Determined by the type of bleeding episode |
Perioperative Management | 50 - 100 | Determined by the type of surgical intervention |
Routine Prophylaxis | 85 | Every other day |
A guide for dosing FEIBA is provided in
Dose (unit/kg) | Frequency of Doses (hours) | Duration of Therapy | |
Control and Prevention of Bleeding | |||
Joint Hemorrhage | 50 - 100 | 12 | Until pain and acute disabilities are improved. |
Mucous Membrane Bleeding | 50 - 100 | 6 | At least 1 day or until bleeding is resolved. |
Soft Tissue Hemorrhage (e.g., retroperitoneal bleeding) | 100 | 12 | Until resolution of bleed. |
Other Severe Hemorrhage (e.g., CNS bleeds) | 100 | 6 - 12 | Until resolution of bleed. |
Perioperative Management | |||
Preoperative | 50 - 100 | One time dose | Immediately prior to surgery. |
Postoperative | 50 - 100 | 6 - 12 | Until resolution of bleed and healing is achieved. |
Routine Prophylaxis | |||
85 | Every other day |
For intravenous injection or intravenous infusion after reconstitution only.
FEIBA is available as a lyophilized powder in single-use glass vials containing nominally 500, 1000, or 2500 units per vial.
FEIBA is available as a lyophilized powder in single-use vials containing nominally 500, 1000, or 2500 units per vial.
Thromboembolic events (including venous thrombosis, pulmonary embolism, myocardial infarction, and stroke) can occur with FEIBA, particularly following the administration of high doses (above 200 units per kg per day) and/or in patients with thrombotic risk factors [see Adverse Reactions (
Patients with DIC, advanced atherosclerotic disease, crush injury, septicemia, or concomitant treatment with recombinant factor VIIa have an increased risk of developing thrombotic events due to circulating tissue factor or predisposing coagulopathy. Potential benefit of treatment with FEIBA should be weighed against the potential risk of these thromboembolic events.
Monitor patients receiving more than 100 units per kg of body weight of FEIBA for the development of DIC, acute coronary ischemia and signs and symptoms of other thromboembolic events. If clinical signs or symptoms occur, such as chest pain or pressure, shortness of breath, altered consciousness, vision, or speech, limb or abdomen swelling and/or pain, discontinue the infusion and initiate appropriate diagnostic and therapeutic measures.
Hypersensitivity and allergic reactions, including severe anaphylactoid reactions, can occur following the infusion of FEIBA. The symptoms include urticaria, angioedema, gastrointestinal manifestations, bronchospasm, and hypotension. These reactions can be severe and systemic. Other infusion reactions, such as chills, pyrexia, and hypertension have also been reported. If signs and symptoms of severe allergic reactions occur, immediately discontinue administration of FEIBA and provide appropriate supportive care.
Because FEIBA is made from human plasma it may carry a risk of transmitting infectious agents, e.g., viruses, and the variant Creutzfeldt-Jakob disease (vCJD) agent and, theoretically, the Creutzfeldt-Jakob disease (CJD) agent. The risk has been minimized by screening plasma donors for prior exposure to certain viruses, by testing for the presence of certain current virus infections and by inactivating and removing certain viruses during the manufacturing process [see Description (
All infections thought by a physician to have been possibly transmitted by this product should be reported by the physician or other healthcare providers to Baxalta US Inc., at 1-800-423-2090 (in the U.S.) and /or to FDA Med Watch (1-800-FDA-1088 or www.fda.gov/medwatch).
The most frequently reported adverse reactions observed in >5% of subjects in the prophylaxis trial were anemia, diarrhea, hemarthrosis, hepatitis B surface antibody positive, nausea, and vomiting.
The serious adverse reactions seen with FEIBA are hypersensitivity reactions and thromboembolic events, including stroke, pulmonary embolism and deep vein thrombosis.
To report SUSPECTED ADVERSE REACTIONS, contact Baxalta US Inc. at 1-800-999-1785 or FDA at 1-800-FDA-1088 or
Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in clinical practice.
The safety assessment of FEIBA is based on the review of the data from two prospective clinical trials in which FEIBA was used for the treatment of acute bleeding episodes and a prospective trial that compared the use of FEIBA prophylactically versus on-demand treatment.
The adverse reactions reported from two prospective clinical trials in which FEIBA was used for the treatment of acute bleeding episodes were chills, chest pain, chest discomfort, dizziness, dysgeusia, dyspnea, hypoesthesia, increase of inhibitor titer (anamnestic response), nausea, pyrexia, and somnolence. Specifically, the first trial was a multicenter randomized, double-blind trial in 15 hemophilia A subjects with inhibitors to factors VIII. The second trial was a multicenter FEIBA study conducted in 44 hemophilia A subjects with inhibitors, 3 hemophilia B subjects with inhibitors and 2 acquired factor VIII inhibitor subjects. Of the 489 infusions used to treat acute bleeds during the second trial, 18 (3.7%) caused minor transient reactions of chills, fever, nausea, dizziness and dysgeusia. Out of 49 subjects, 10 (20%) had a rise in their inhibitor titers after treatment with FEIBA. Five of these subjects (50%) had increases that were, tenfold or more, and 3 (30%) of these subjects received factor VIII or IX concentrates within 2 weeks prior to treatment with FEIBA. These anamnestic rises were not associated with decreased efficacy of FEIBA.
MedDRA System Organ Class | Preferred Term | Number of ARs | Number of Subjects | Percent of Subjects (N=36) |
---|---|---|---|---|
Blood And Lymphatic System Disorders | Anemia | 2 | 2 | 5.6 |
Gastrointestinal Disorders | Diarrhea | 2 | 2 | 5.6 |
Nausea | 2 | 2 | 5.6 | |
Vomiting | 2 | 2 | 5.6 | |
Investigations | Hepatitis B Surface Antibody Positive | 4 | 4 | 11.1 |
Musculoskeletal And Connective Tissue Disorders | Hemarthrosis | 5 | 3 | 8.3 |
Because post-marketing reporting of adverse reactions is voluntarily and from a population of uncertain size, it is not always possible to reliably estimate the frequency of these reactions or establish a causal relationship to product exposure.
Concomitant Medications
Consider the possibility of thrombotic events when systemic antifibrinolytics such as tranexamic acid and aminocaproic acid are used during treatment with FEIBA. No adequate and well-controlled studies of the combined or sequential use of FEIBA and recombinant factor VIIa or antifibrinolytics have been conducted. Use of antifibrinolytics within approximately 6 to 12 hours after the administration of FEIBA is not recommended.
Consider the possibility of thrombotic events when systemic antifibrinolytics such as tranexamic acid and aminocaproic acid are used. Use of antifibrinolytics within approximately 6 to 12 hours after the administration of FEIBA is not recommended.
Pregnancy Category C
Animal reproduction studies have not been conducted with FEIBA. There are no adequate and well-controlled studies in pregnant women. It is also not known whether FEIBA can cause fetal harm when administered to a pregnant woman or can affect reproductive capacity. FEIBA should be administered to pregnant women only if clearly needed.
There is no information available on the effect of FEIBA on labor and delivery.
It is not known whether this drug is excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when FEIBA is administered to a nursing woman.
Safety and efficacy of FEIBA have been evaluated in nine pediatric subjects treated in the routine prophylaxis trial including 4 subjects ≥7 to <12 years of age and 5 subjects ≥12 to <16 years of age. The dosing for all pediatric subjects was based on body weight. A total of 576 infusions were given for the treatment of 223 bleeding episodes. In 223 (100%) of the episodes, hemostasis was achieved with one or more infusions. Hemostatic efficacy was rated as excellent or good in a majority (96.9%) of the bleeding episodes in both regimens at 24 hours post infusion. The median annualized bleeding episode rate (ABR) for children ≥7 to <12 years of age was 7.7 bleeds per patient per year, as compared to 39 for subjects treated with on-demand therapy. [see Clinical Studies (
The safety and efficacy of FEIBA has not been evaluated in neonates.
The safety and efficacy of FEIBA has not been evaluated in subjects ≥ 65 years of age.
FEIBA is a freeze-dried sterile human plasma fraction with factor VIII inhibitor bypassing activity to be reconstituted for intravenous administration. Factor VIII inhibitor bypassing activity is expressed in arbitrary units. One unit of activity is defined as that amount of FEIBA that shortens the aPTT of high titer factor VIII inhibitor reference plasma to 50% of the blank value.
FEIBA contains mainly non-activated factors II, IX, and X and mainly activated factor VII. It contains approximately equal unitages of factor VIII inhibitor bypassing activity and prothrombin complex factors. In addition, the preparation contains 1-6 units of factor VIII coagulant antigen (FVIII C:Ag) per mL. The product contains traces of factors of the kinin generating system. It contains no heparin. Reconstituted FEIBA contains 4 mg of trisodium citrate and 8 mg of sodium chloride per mL.
FEIBA is manufactured from large pools of human plasma. Screening against potentially infectious agents begins with the donor selection process and continues throughout plasma collection and plasma preparation. Each individual plasma donation used in the manufacture of FEIBA is collected at FDA approved blood establishments and is tested by FDA licensed serological tests for Hepatitis B Surface Antigen (HBsAg), and for antibodies to Human Immunodeficiency Virus (HIV-1/HIV-2) and Hepatitis C Virus (HCV) Mini-pools of the plasma are tested and found negative for the presence of HIV-1 and HCV by FDA licensed Nucleic Acid Testing (NAT).
To reduce the risk of viral transmission, the manufacturing process of FEIBA includes two dedicated and independent virus removal/inactivation steps namely 35 nm nanofiltration and a vapor heat treatment process. In addition, the DEAE-Sephadex adsorption contributes to the virus safety profile of FEIBA.
In vitro spiking studies have been used to validate the capability of the manufacturing process to remove and inactivate viruses.
Virus Type | Enveloped RNA | Enveloped DNA | Non-enveloped RNA | Non-enveloped DNA | |||
Virus Family | Retroviridae | Flaviviridae | Herpesviridae | Picornaviridae | Parvoviridae | ||
Virus | HIV-1 | BVDV | WNV | PRV | HAV | B19V | MMV |
DEAE Sephadex Adsorption | 3.2 | 1.8 | ND | 2.5 | 1.5 | 1.7 | 1.2 |
35 nm Nanofiltration | > 5.3 | 2.1 | 4.7 | > 5.7 | 2.6 | 0.2 | 1.0 |
Vapor-Heat Treatment | > 5.9 | > 5.6 | > 8.1 | > 6.7 | > 5.2 | 3.5 | 0.9 |
Overall virus reduction factor (log10) | > 14.4 | > 9.5 | > 12.8 | > 14.9 | > 9.3 | 5.2 | 2.2 |
Multiple interactions of the components in FEIBA restore the impaired thrombin generation of hemophilia patients with inhibitors. In vitro, FEIBA shortens the activated partial thromboplastin time of plasma containing factor VIII inhibitor.4,5
Long-term animal studies to evaluate the carcinogenic potential of FEIBA or studies to determine the genotoxicity or the effect of FEIBA on fertility have not been performed. An assessment of the carcinogenic potential of FEIBA was completed to demonstrate minimal carcinogenic risk from product use.
Control and Prevention of Bleeding Episodes
The efficacy of FEIBA in the treatment of bleeding episodes has been demonstrated by two prospective clinical trials1,2.
The first trial was a multicenter, randomized, double-blind trial comparing the effect of FEIBA and a non-activated prothrombin complex concentrate in 15 subjects with hemophilia A and inhibitors to factor VIII. The inclusion criteria were history of high titer inhibitors, high responder status, more than 1 bleeding episode per month in the prior year and no signs of liver failure. A total of 150 bleeding episodes including 117 joint, 20 musculoskeletal and 4 mucocutaneous bleeds, were treated. A single dose of 88 units per kg of body weight was used uniformly for treatments with FEIBA. A second treatment was allowed for muscle bleeds after 12 hours and 6 hours after mucocutaneous bleeds, if necessary
Subjects and investigators were asked to rate hemostatic efficacy based on a scale of effective, partially effective, not effective or not sure. The criteria for evaluation of the effectiveness were severity of pain, subjective improvement, circumference of muscle or joint, restriction of joint mobility, cessation of open bleeding, start of rebleeding and quantity and nature of analgesics. FEIBA was effective in 41% and partly effective in 25% of episodes, while prothrombin complex concentrate was rated effective in 25% and partly effective in 21% of episodes (i.e., combined effectiveness of 46%).
The second trial with FEIBA was a multicenter randomized, prospective trial. This trial was conducted in 44 hemophilia A subjects with inhibitors, 3 hemophilia B subjects with inhibitors and 2 acquired factor VIII inhibitor subjects. It was designed to evaluate the efficacy of FEIBA in the treatment of joint, mucous membrane, musculocutaneous and emergency bleeding episodes such as central nervous system hemorrhages and surgical bleedings. The inclusion criteria used were age >4 years, history of inhibitor titer ≥4 BU and without chronic liver disease. Subjects were excluded if they had a history of thromboembolic events or allergic reactions to FEIBA.
Forty-nine (49) subjects with inhibitor titers of greater than 5 Bethesda Units were enrolled from nine co-operating hemophilia centers. Subjects were treated with 50 units per kg of body weight, repeated at 12-hour intervals (6-hour intervals in mucous membrane bleedings), if necessary. A total of 489 infusions were given for the treatment of 165 bleeding episodes (102 joint, 33 muscle and soft tissue, 20 mucous membrane, and 10 emergency bleeds, including 3 central nervous system bleeds and 4 surgical procedures). Bleeding was controlled in 153 episodes (93%). In 130 (78%) of the episodes, hemostasis was achieved with one or more infusions within 36 hours. Of these, 36% were controlled with one infusion within 12 hours. An additional 14% of episodes responded after more than 36 hours.
Routine Prophylaxis
In a multicenter, open-label, prospective, randomized clinical trial comparing subjects receiving FEIBA for prophylaxis with subjects receiving FEIBA for on-demand treatment, 36 hemophilia A and B subjects with inhibitors to factor VIII or IX were analyzed in the intent-to-treat analysis. Study population included 29 (80.6%) Caucasian, 3 (8.3%) Asian, 2 (5.6%) Black/African American, and 2 (5.6%) other. Inclusion criteria were subjects with a history of high titer inhibitors or low titer refractory to increased factor VIII or IX dosing, age range between 4 and 65, and subjects receiving bypassing agents with ≥12 bleeds in the 12 months prior to trial entry. Subjects with a history of thromboembolic events, symptomatic liver disease, or a platelet count <100,000 per mL, and those receiving immune tolerance induction or routine prophylaxis were excluded.
Subjects were randomized to receive 12 months of prophylactic or on-demand treatment with FEIBA. Seventeen subjects randomized to the prophylaxis arm received 85 units per kg of FEIBA every other day. Nineteen subjects randomized to the on-demand arm received FEIBA for the treatment of acute bleeding episodes per the dose and dosing regimen recommended. Target joints were defined as ≥4 bleeding episodes within 6 months. In this trial, ankles, knees, elbows and hips were target joint locations. Preexisting target joints were not considered as new target joints.
Hemostatic efficacy for treatment of acute bleeds was evaluated at 6 and 24 hours according to a pre-specified four-point scale of excellent, good, fair, or none. An evaluation of “none” was considered a treatment failure. The criteria for evaluation of the effectiveness were relief of pain, cessation of bleeding, and number of infusions required to treat a bleed.
A total of 825 bleeding episodes were reported including 196 that occurred during prophylaxis and 629 that occurred during on-demand therapy. A majority (78%) of the 794 bleeding episodes that were rated for efficacy were treated with 1 or 2 infusions. Hemostatic efficacy was rated as excellent or good for 74% of bleeding episodes rated at 6 hours post infusion and for 87% of the bleeding episodes at 24 hour post infusion. A total of 19 (2.4%) bleeds were rated as “none” at 6 hours post infusion; 1 bleed (0.1%) was rated “none” at 24 hours.
Hemostatic efficacy for routine prophylaxis was evaluated against subjects who received on-demand therapy.
The overall median annual bleed rate (ABR) for the on-demand arm was 28.7 compared to 7.9 for the prophylaxis arm, which represents a 72% reduction in median ABR with prophylaxis. When analyzed by site (e.g. joint, non-joint) and cause of bleed (e.g. spontaneous, traumatic), prophylactic treatment with FEIBA resulted in a greater than 50% reduction in ABR. There were fewer subjects in the prophylaxis arm who developed new target joints (7 new target joints in 5 subjects treated with prophylaxis compared to 23 new target joints in 11 subjects in the on-demand arm). Target joints developed in two subjects in the on-demand arm and three in the prophylaxis arm who did not have reported target joints at trial enrollment. A total of 3 of 17(18%) subjects had no bleeding episodes on prophylaxis. In the on-demand arm, all subjects experienced a bleeding episode.
ABR by age category between on-demand and prophylaxis regimens is provided in
Age Category | On-Demand | Prophylaxis | ||
Number of Subjects | ABR Median | Number of Subjects | ABR Median | |
Children (≥7 to <12 years old) | 2 | 39.3 | 2 | 7.7 |
Adolescent (≥12 to <16 years old) | 2 | 30.9 | 3 | 27.5 |
Adult (≥16 years old) | 15 | 23.9 | 12 | 6.9 |
How Supplied
FEIBA is available in single-dose vials in the following nominal dosage strengths:
Nominal Strength | Color Code | Factor VIII Potency Range | Kit NDC | Sterile Water Volume |
500 units | Blue | 350-650 units per vial | 64193-426-02 | 10 mL |
1000 units | Green | 700-1300 units per vial | 64193-424-02 | 20 mL |
2500 units | Purple | 1750-3250 units per vial | 64193-425-02 | 50 mL |
The number of units of factor VIII inhibitor bypassing activity is stated on the label of each vial.
FEIBA is packaged with a suitable volume of Sterile Water for Injection, U.S.P., one BAXJECT II Hi-Flow Needleless Transfer Device, and one Package Insert.
Storage and Handling
To enroll in the confidential, Industry-wide Patient Notification System, call 1-888-873-2838.
Baxalta and Feiba are trademarks of Baxalta Incorporated.
Baxalta US Inc.
Westlake Village, CA 91362 USA
U.S. License No. 2020
Single-dose vial
NDC 64193-426-02
Anti-Inhibitor Coagulant Complex
FEIBA
Nanofiltered & Vapor Heated
Warning: This is a potent drug with potential hazards.
For maximal safety and efficacy, carefully read and follow enclosed directions.
This product is prepared from large pools of human plasma. Human blood and its components may transmit infectious agents. The physician and the patient should discuss the risks and benefits of this product.
The product has been subjected to in-process virus inactivation. See package insert for details.
Feiba, Baxalta and Baxject are trademarks of Baxalta Incorporated.
*No U.S. standard of potency.
Single-dose vial
NDC 64193-326-01
Anti-Inhibitor Coagulation Complex
FEIBA
Nanofiltered & Vapor Heated
For Intravenous Use After Reconstitution
No preservative
Dosage & Administration: See accompanying package insert.
Storage: Room temperature not to exceed 25°C (77°F).
Reconstitution: Use 10 mL sWFI, U.S.P.; Keep at room temperature not to exceed 25°C (77°F); Use within 3 hours of reconstitution.
Rx only
FEIBA Anti-Inhibitor Coagulant Complex 500 U Unit Carton FEIBA Anti-Inhibitor Coagulant Complex 500 U Vial Label
20 mL size, dried
NDC 64193-424-02
Anti-Inhibitor Coagulant Complex
FEIBA
Nanofiltered & Vapor Heated
Warning: This is a potent drug with potential hazards.
For maximal safety and efficacy, carefully read and follow enclosed directions.
This product is prepared from large pools of human plasma. Human blood and its components may transmit infectious agents. The physician and the patient should discuss the risks and benefits of this product.
The product has been subjected to in-process virus inactivation. See package insert for details.
Feiba, Baxalta and Baxject are trademarks of Baxalta Incorporated.
*No U.S. standard of potency.
20 ml size, dried
NDC 64193-324-01
Anti-Inhibitor Coagulation Complex
FEIBA
Nanofiltered & Vapor Heated
For Intravenous Use After Reconstitution
Contains no preservatives
Dosage & Administration: See accompanying package insert.
Storage: Room temperature not to exceed 25°C (77°F).
Reconstitution: Use 20 mL sWFI, U.S. P.; Keep at room temperature not to
exceed 25°C (77°F); Use within 3 hours of reconstitution.
Rx only
NDC 64193-424-02 20 mL carton label NDC 64193-324-01 20 mL vial label
50 mL size, dried
NDC 64193-425-02
Anti-Inhibitor Coagulant Complex
FEIBA
Nanofiltered & Vapor Heated
Warning: This is a potent drug with potential hazards.
For maximal safety and efficacy, carefully read and follow enclosed directions.
This product is prepared from large pools of human plasma. Human blood and its components may transmit infectious agents. The physician and the patient should discuss the risks and benefits of this product.
The product has been subjected to in-process virus inactivation. See package insert for details.
Feiba, Baxalta and Baxject are trademarks of Baxalta Incorporated.
*No U.S. standard of potency.
50 ml size, dried
NDC 64193-325-01
Anti-Inhibitor Coagulation Complex
FEIBA
Nanofiltered & Vapor Heated
For Intravenous Use After Reconstitution
Contains no preservatives
Dosage & Administration: See accompanying package insert.
Storage: Room temperature not to exceed 25°C (77°F).
Reconstitution: Use 50 mL sWFI, U.S. P.; Keep at room temperature not to
exceed 25°C (77°F); Use within 3 hours of reconstitution.
Rx only
NDC 64193-425-02 50 mL carton label NDc 64193-325-01 50 mL vial label
10 mL
NDC 52919-005-05
Sterile Water for Injection, USP
for reconstitution of accompanying product
Do not use unless clear. No antimicrobial agent or other substance has been added. Do not use for intravascular injection without making approximately isotonic by addition of suitable solute. Discard unused portion.
Rx Only.
Single dose container
Nonpyrogenic
NDC 52919-006-05
Nonpyrogenic
Single-Dose Container
Sterile Water for Injection, USP
for reconstitution of accompanying product
Do not use unless clear. No antimicrobial agent or other
substance has been added. Do not use for intravascular
injection without making approximately isotonic by
addition of suitable solute. Discard unused portion.
Rx Only.
Manufactured for Baxalta US Inc.
Westlake Village, CA 91362
Nonpyrogenic
NDC 0338-0001-65
50 ml
Single-Dose Container
Baxter
Sterile Water for Injection, USP
for reconstitution of accompanying product
See accompanying directions for use. Do not use unless clear. No antimicrobial
agent or other substance has been added. Do not use for intravascular injection
without making approximately isotonic by addition of suitable solute. Discard unused portion.
Rx Only.
Manufactured by
Baxter Healthcare Corporation
Deerfield, IL 60015 USA
Imported by
Baxter Corporation
Mississauga, ON L5N 0C2
Baxter is a trademark of Baxter International Inc.
Sterile Water for Injection, USP 10 mL 20 mL Sterile Water Label Sterile Water for Injection, USP 50mL
Depending on the reaction of the Anti-Inhibitor Coagulant Complex after taken, if you are feeling dizziness, drowsiness or any weakness as a reaction on your body, Then consider Anti-Inhibitor Coagulant Complex not safe to drive or operate heavy machine after consumption. Meaning that, do not drive or operate heavy duty machines after taking the capsule if the capsule has a strange reaction on your body like dizziness, drowsiness. As prescribed by a pharmacist, it is dangerous to take alcohol while taking medicines as it exposed patients to drowsiness and health risk. Please take note of such effect most especially when taking Primosa capsule. It's advisable to consult your doctor on time for a proper recommendation and medical consultations.
Is Anti-Inhibitor Coagulant Complex addictive or habit forming?Medicines are not designed with the mind of creating an addiction or abuse on the health of the users. Addictive Medicine is categorically called Controlled substances by the government. For instance, Schedule H or X in India and schedule II-V in the US are controlled substances.
Please consult the medicine instruction manual on how to use and ensure it is not a controlled substance.In conclusion, self medication is a killer to your health. Consult your doctor for a proper prescription, recommendation, and guidiance.
Visitors | % | ||
---|---|---|---|
1-5mg | 1 | 100.0% |
There are no reviews yet. Be the first to write one! |
The information was verified by Dr. Rachana Salvi, MD Pharmacology