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Acemin Side Effects

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Common Acemin Side Effects


The most commonly reported Acemin side effects (click to view or check a box to report):

Gangrene (2)
Pseudomonas Infection (2)
Peripheral Arterial Occlusive Disease (2)
Hyperkalaemia (2)
Renal Failure (2)
Intermittent Claudication (2)
Metastases To Lung (2)
Pain In Extremity (2)
Dizziness (1)
Diarrhoea (1)
Enteritis Infectious (1)
Tonsillitis (1)
Anaphylactic Shock (1)
Tonsillectomy (1)
Circulatory Collapse (1)
Depressed Level Of Consciousness (1)
Blood Glucose Increased (1)
Blood Glucose Abnormal (1)
Arthropod Bite (1)
Arterial Occlusive Disease (1)

➢ More



If you or someone in your family has experienced a serious side effect to a health product, you are encouraged to report the experience to your health care professional (e.g. physician, pharmacist). You could also complete a copy of the side effect reporting form or report your side effect to FDA.

Acemin Side Effects Reported to FDA



Acemin Side Effect Report#9536106
Arthropod Bite, Circulatory Collapse, Head Injury, Hypertensive Crisis, Joint Injury, Anaphylactic Shock, Syncope, Labile Blood Pressure
This is a report of a male patient (weight: NA) from AT, suffering from the following health symptoms/conditions: hypertension, who was treated with Acemin (dosage: 5 Mg, Daily, Cumulative Dose To The First Reaction: 14610 Mg, start time: 2005), combined with:
  • Casodex (8 Month, Day/one)
  • Casodex (8 Month, Day/one)
  • Aerius (Two Weeks Daily)
  • Listerine Mouthwash (Daily, Used More That One Year)
  • Concor
  • Acecomb
and developed a serious reaction and side effect(s): Arthropod Bite, Circulatory Collapse, Head Injury, Hypertensive Crisis, Joint Injury, Anaphylactic Shock, Syncope, Labile Blood Pressure after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Acemin treatment in male patients, resulting in Arthropod Bite side effect. The patient was hospitalized.
Acemin Side Effect Report#7450558-3
Peripheral Arterial Occlusive Disease, Pain In Extremity, Metastases To Lung, Intermittent Claudication, Pseudomonas Infection, Femoral Artery Occlusion, Gangrene, Metastatic Renal Cell Carcinoma, Blood Glucose Increased
This report suggests a potential Acemin Peripheral Arterial Occlusive Disease side effect(s) that can have serious consequences. A 68-year-old male patient (weight: NA) from Austria was diagnosed with the following symptoms/conditions: peripheral arterial occlusive disease and used Acemin (dosage: 5 Mg, Bid) starting
Jan 01, 2009. After starting Acemin the patient began experiencing various side effects, including: Peripheral Arterial Occlusive Disease, Pain In Extremity, Metastases To Lung, Intermittent Claudication, Pseudomonas Infection, Femoral Artery Occlusion, Gangrene, Metastatic Renal Cell Carcinoma, Blood Glucose IncreasedAdditional drugs used concurrently:
  • Marcoumar (Unk)
  • Tasigna (800 Mg, 200 X 4)
  • Plavix (75 Mg, Bid)
The patient was hospitalized and became disabled. Although Acemin demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Peripheral Arterial Occlusive Disease, may still occur.
Acemin Side Effect Report#7413504-4
Gangrene, Metastases To Lung, Neoplasm Malignant, Peripheral Ischaemia, Peripheral Arterial Occlusive Disease, Intermittent Claudication, Arterial Occlusive Disease, Pseudomonas Infection, Pain In Extremity
This Gangrene problem was reported by a physician from Austria. A 67-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: peripheral arterial occlusive disease. On
Jan 01, 2009 this consumer started treatment with Acemin (dosage: 5 Mg, Bid). The following drugs were being taken at the same time:
  • Marcoumar (Unk)
  • Tasigna (800 Mg, 200 X 4)
  • Plavix (75 Mg, Bid)
When using Acemin, the patient experienced the following unwanted symptoms/side effects: Gangrene, Metastases To Lung, Neoplasm Malignant, Peripheral Ischaemia, Peripheral Arterial Occlusive Disease, Intermittent Claudication, Arterial Occlusive Disease, Pseudomonas Infection, Pain In ExtremityThe patient was hospitalized and became disabled.Although all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Gangrene, may become evident only after a product is in use by the general population.
Acemin Side Effect Report#7206391-0
Enteritis Infectious, Tonsillectomy, Diarrhoea, Vomiting, Tonsillitis
This Enteritis Infectious side effect was reported by a physician from Austria. A female patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Acemin (drug dosage: NA), which was initiated on
Jul 05, 2007. Concurrently used drugs:
  • Augmentin '125' (1 G, Bid)
  • Acecomb
  • Dilatrend (Unk, Unk)
  • Augmentin '125' (650 Mg, Bid)
  • Normoxin
  • Certican (Unk)
  • Isradipine
.After starting to take Acemin the consumer reported adverse symptoms, such as: Enteritis Infectious, Tonsillectomy, Diarrhoea, Vomiting, TonsillitisThese side effects may potentially be related to Acemin. The patient was hospitalized.
Acemin Side Effect Report#6506519-1
Blood Glucose Abnormal, Depressed Level Of Consciousness, Dizziness, Loss Of Consciousness
This is a report of a 67-year-old female patient (weight: NA) from Austria, suffering from the following health symptoms/conditions: NA, who was treated with Acemin (dosage: NA, start time: NS), combined with:
  • Dilatrend
  • Doxapress
and developed a serious reaction and side effect(s): Blood Glucose Abnormal, Depressed Level Of Consciousness, Dizziness, Loss Of Consciousness after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Acemin treatment in female patients, resulting in Blood Glucose Abnormal side effect. The patient was hospitalized.
Acemin Side Effect Report#6388718-5
Hyperkalaemia, Renal Failure
This report suggests a potential Acemin Hyperkalaemia side effect(s) that can have serious consequences. A 84-year-old male patient (weight: NA) from Austria was diagnosed with the following symptoms/conditions: NA and used Acemin (dosage: NA) starting NS. After starting Acemin the patient began experiencing various side effects, including: Hyperkalaemia, Renal FailureAdditional drugs used concurrently:
  • Lasix
  • Spirobene
  • Fedip (If Required)
  • Inotyol (If Required)
  • Metoclopramide Hydrochloride (4 Mg/ml, If Required)
  • Seloken Retard (95 Mg, 0.5 Df Twice A Day)
  • Tramal Retard (If Required)
The patient was hospitalized. Although Acemin demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Hyperkalaemia, may still occur.
Acemin Side Effect Report#6384962-1
Hyperkalaemia, Renal Failure
This Hyperkalaemia problem was reported by a physician from Austria. A 84-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On NS this consumer started treatment with Acemin (dosage: NA). The following drugs were being taken at the same time:
  • Lasix
  • Spirobene
  • Fedip (If Required)
  • Inotyol (If Required)
  • Metoclopramide Hydrochloride (4 Mg/ml, If Required)
  • Seloken Retard (95 Mg, 0.5 Df Twice A Day)
  • Tramal Retard (If Required)
When using Acemin, the patient experienced the following unwanted symptoms/side effects: Hyperkalaemia, Renal FailureThe patient was hospitalized.Although all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Hyperkalaemia, may become evident only after a product is in use by the general population.
Acemin Side Effect Report#5126711-0
Local Swelling, Oedema Mouth
This Local Swelling side effect was reported by a health professional from Austria. A 94-year-old female patient (weight:NA) experienced the following symptoms/conditions: hypertension.The patient was prescribed Acemin (drug dosage: NA), which was initiated on
Jan 01, 2001. Concurrently used drugs:
  • Fosamax
  • Madopar (100 Mg/25 Mg)
  • Moxonibene
  • Seropram
  • Thrombo Ass
  • Trittico Ret
.After starting to take Acemin the consumer reported adverse symptoms, such as: Local Swelling, Oedema MouthThese side effects may potentially be related to Acemin.



The appearance of Acemin on this list does not mean that FDA has concluded that the drug has the listed risk. It means that FDA has identified a potential safety issue, but it does not mean that FDA has found a causal relationship between the drug and the listed risk.

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Track Your Side Effects

Note Your Observations

It is really important to keep track of your health symptoms, right from the time you start a new medicine. You can do it any way you prefer: in a notebook, in a computer file or using our online tool. You should also note down any other medicines you are taking at the same time, because there could be an interaction between these medicines.

Why Your Notes are Important

Your notes could be helpful in several ways:

  • You can use them to remind you of details that may alert your health care professional(s) to a problem
  • You will have a record to refer to in the future, in case you are ever prescribed the same medicine again

  • Log Form

    You can use the following log form to write down important information, like the date and time you experienced a side effect and your symptoms, how strong the symptoms were, and any other medicines you were using.

    Medicine Name and Dosage:
    Side Effects Scale Date & Time Other Medicine(s) or Treatment(s)
    Scale: 1 = very mild to 10 = very bad

    Side effects reports are analyzed to discover potential health product safety signals. Some important reactions may take an extremely long time to develop or occur infrequently. Continued monitoring of adverse reactions is thus essential to maintain a comprehensive safety and effectiveness profile of health products.

    You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.

    Acemin reports list potential signals of serious risks and new safety information that were identified using the FDA Adverse Event Reporting System (FAERS).
    FAERS is a database that contains information on adverse event and medication errors reports submitted to FDA by healthcare professionals (such as physicians, pharmacists, nurses and others), consumers (such as patients, family members, layers and others) and manufacturers.

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    Acemin Safety Alerts, Active Ingredients, Usage Information

    More About Acemin

    Side Effects reported to FDA: 8

    Acemin safety alerts: No

    Reported hospitalizations: 7

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