APIDRA Side Effects

6688632-1 | Eye Haemorrhage, Hyperglycaemia
on Apr 15, 2010 Female patient from BRAZIL , weighting 154.3 lb, was diagnosed with type 2 diabetes mellitus and was treated with Apidra (View Usage). Patient experienced the following unwanted or unexpected effects: eye haemorrhage, hyperglycaemia. Apidra dosage: According To Cho Count.. During the same period patient was treated with AUTOPEN 24 (View Autopen 24 Review and Autopen 24 Label ), LANTUS (View Lantus Review and Lantus Label ), NOVORAPID (According To Cho Count.) (View Novorapid Review and Novorapid Label ), ATENSINA (View Atensina Review and Atensina Label ), AMLODIPINE (View Amlodipine Review and Amlodipine Label ).

6688628-X | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Decreased Appetite, Gamma-glutamyltransferase Increased, Hepatic Function Abnormal, Malaise
Patient was taking Apidra (View Usage). Patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, decreased appetite, gamma-glutamyltransferase increased, hepatic function abnormal, malaise on Apr 14, 2010 from JAPAN Additional patient health information: Male patient , 77 years of age, weighting 137.8 lb, was diagnosed with diabetes mellitus, hypertension and. Apidra dosage: Dose:4 Unit(s). During the same period patient was treated with LANTUS (Dose:6 Unit(s)) (View Lantus Review and Lantus Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), NORVASC (View Norvasc Review and Norvasc Label ), FLUVASTATIN (View Fluvastatin Review and Fluvastatin Label ), CANDESARTAN CILEXETIL (View Candesartan Cilexetil Review and Candesartan Cilexetil Label ), SIGMART (View Sigmart Review and Sigmart Label ), ARTIST (View Artist Review and Artist Label ), ZETIA (View Zetia Review and Zetia Label ). Patient was hospitalized.

6683279-5 | Myelitis
Adverse event was reported on Apr 09, 2010 by a Female patient taking Apidra (View Usage) (Dosage: The Dose Of Once' 16-20 Units; Tid Dose:16 Unit(s)) . Location: JAPAN , 29 years of age, weighting 153.0 lb, After Apidra was administered, patient had the following side effects: myelitis. During the same period patient was treated with LANTUS (Dose:25 Unit(s)) (View Lantus Review and Lantus Label ). Patient was hospitalized.

6653588-4 | Condition Aggravated, Diabetic Retinopathy
on Mar 22, 2010 Male patient from UNITED STATES , 45 years of age, was treated with Apidra (View Usage). Patient experienced the following unwanted or unexpected effects: condition aggravated, diabetic retinopathy. Apidra dosage: Takes Insulin On Sliding Scale ;average 8 Units. During the same period patient was treated with OPTICLICK (View Opticlick Review and Opticlick Label ).


6648949-3 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Decreased Appetite, Gamma-glutamyltransferase Increased, Hepatic Function Abnormal, Malaise
on Mar 18, 2010 Male patient from JAPAN , 77 years of age, weighting 137.8 lb, was diagnosed with diabetes mellitus, hypertension and was treated with Apidra (View Usage). Patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, decreased appetite, gamma-glutamyltransferase increased, hepatic function abnormal, malaise. Apidra dosage: Dose:4 Unit(s). During the same period patient was treated with LANTUS (Dose:6 Unit(s)) (View Lantus Review and Lantus Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), NORVASC (View Norvasc Review and Norvasc Label ), FLUVASTATIN (View Fluvastatin Review and Fluvastatin Label ), CANDESARTAN CILEXETIL (View Candesartan Cilexetil Review and Candesartan Cilexetil Label ), SIGMART (View Sigmart Review and Sigmart Label ), ARTIST (View Artist Review and Artist Label ), ZETIA (View Zetia Review and Zetia Label ). Patient was hospitalized.

6640234-9 | Fall, Femur Fracture
Patient was taking Apidra (View Usage). After Apidra was administered, patient had the following side effects: fall (What is fall?), femur fracture on Mar 13, 2010 from UNITED STATES Additional patient health information: Male patient , 75 years of age, was diagnosed with type 2 diabetes mellitus and. Apidra dosage: Sliding Scale. During the same period patient was treated with LANTUS (Dose:12 Unit(s)) (View Lantus Review and Lantus Label ), OPTICLICK (View Opticlick Review and Opticlick Label ).

6609692-X | Polyneuropathy
Adverse event was reported on Feb 24, 2010 by a Female patient taking Apidra (View Usage) (Dosage: The Dose Of Once' 16-20 Units; Tid) . Location: JAPAN , 29 years of age, weighting 153.0 lb, Patient experienced the following unwanted or unexpected effects: polyneuropathy. During the same period patient was treated with LANTUS (View Lantus Review and Lantus Label ). Patient was hospitalized.

6596631-3 | Eye Swelling, Flushing, Pruritus, Skin Burning Sensation
on Feb 22, 2010 Female patient from UNITED STATES , weighting 213.4 lb, was diagnosed with diabetes mellitus inadequate control and was treated with Apidra (View Usage). Patient had the following side effects: eye swelling, flushing, pruritus, skin burning sensation. Apidra dosage: 5-10 Units At Meals Tid Subcutaneous.

6594667-X | Hypertension, Pruritus, Rash
on Feb 15, 2010 Male patient from UNITED STATES , 87 years of age, was diagnosed with type 2 diabetes mellitus and was treated with Apidra (View Usage). After Apidra was administered, patient had the following side effects: hypertension, pruritus, rash (What is rash?). Apidra dosage: 2-12 Units Taken With Each Meal. During the same period patient was treated with LANTUS (Dose:28 Unit(s)) (View Lantus Review and Lantus Label ), OPTICLICK (View Opticlick Review and Opticlick Label ), SOLOSTAR (View Solostar Review and Solostar Label ), PLAVIX (View Plavix Review and Plavix Label ). Patient was hospitalized.

6583413-1 | Blood Glucose Increased, Cardiac Disorder, Hypertension
Patient was taking Apidra (View Usage). Patient experienced the following unwanted or unexpected effects: blood glucose increased, cardiac disorder, hypertension on Feb 09, 2010 from UNITED STATES Additional patient health information: Female patient , 48 years of age, was diagnosed with diabetes mellitus and. Apidra dosage: With Meals Dose:10 Unit(s). During the same period patient was treated with OPTICLICK (View Opticlick Review and Opticlick Label ). Patient was hospitalized.

6576799-5 | Polyneuropathy
Adverse event was reported on Feb 04, 2010 by a Female patient taking Apidra (View Usage) (Dosage: The Dose Of Once' 16-20 Units; Tid) . Location: JAPAN , 29 years of age, weighting 153.0 lb, Patient had the following side effects: polyneuropathy. During the same period patient was treated with LANTUS (Dose:30 Unit(s)) (View Lantus Review and Lantus Label ). Patient was hospitalized.

6567147-5 | Infection, Sepsis
on Jan 22, 2010 Male patient from UNITED STATES , 62 years of age, was diagnosed with type 2 diabetes mellitus and was treated with Apidra (View Usage). After Apidra was administered, patient had the following side effects: infection (What is infection?), sepsis (What is sepsis?). Apidra dosage: With Meals Dose:4 Unit(s). During the same period patient was treated with OPTICLICK (View Opticlick Review and Opticlick Label ).

6565066-1 | Erythema, Fall, Injection Site Nodule, Injection Site Pain, Pruritus, Trigger Finger, Wrist Fracture
on Jan 19, 2010 Female patient from UNITED STATES , 70 years of age, was treated with Apidra (View Usage). Patient experienced the following unwanted or unexpected effects: erythema, fall (What is fall?), injection site nodule, injection site pain, pruritus, trigger finger, wrist fracture. Apidra dosage: Dose:10 Unit(s). During the same period patient was treated with INSULIN DETEMIR (Dose As Used: 35 Units In A.m. And 78 Units In P.m.) (View Insulin Detemir Review and Insulin Detemir Label ), LANTUS (Dose:60 Unit(s)) (View Lantus Review and Lantus Label ), HUMALOG (View Humalog Review and Humalog Label ).

6477434-7 | Myocardial Infarction
Patient was taking Apidra (View Usage). Patient had the following side effects: myocardial infarction on Oct 12, 2009 from AUSTRALIA Additional patient health information: Female patient , 58 years of age, . Apidra dosage: .

6419730-5 | Contusion, Eye Disorder, Fall, Feeling Abnormal, Feeling Cold, Headache, Hemiplegia, Hyperglycaemia, Hyperhidrosis
Adverse event was reported on Oct 22, 2009 by a Female patient taking Apidra (View Usage) (Dosage: Dose: Via Pump, Approximately 11.3 Units Daily) . Location: UNITED STATES , 57 years of age, weighting 130.1 lb, After Apidra was administered, patient had the following side effects: contusion, eye disorder, fall (What is fall?), feeling abnormal, feeling cold, headache (What is headache?), hemiplegia, hyperglycaemia, hyperhidrosis.

6415658-5 | Scar, Weight Decreased
on Oct 20, 2009 Male patient from BRAZIL , 53 years of age, weighting 154.3 lb, was treated with Apidra (View Usage). Patient experienced the following unwanted or unexpected effects: scar (What is scar?), weight decreased. Apidra dosage: Dose: Acc To Glycemia. During the same period patient was treated with LANTUS (View Lantus Review and Lantus Label ), METFORMIN HCL (View Metformin Hcl Review and Metformin Hcl Label ). Patient was hospitalized.

6414053-2 | Product Quality Issue
on Oct 19, 2009 Female patient from FINLAND , 70 years of age, was diagnosed with hypertension and was treated with Apidra (View Usage). Patient had the following side effects: product quality issue. Apidra dosage: Dose: 2-6. During the same period patient was treated with LANTUS (View Lantus Review and Lantus Label ), ATENOL (View Atenol Review and Atenol Label ), ANAFRANIL SR (View Anafranil Sr Review and Anafranil Sr Label ), DIFORMIN (View Diformin Review and Diformin Label ), CRESTOR (View Crestor Review and Crestor Label ), PLAVIX (View Plavix Review and Plavix Label ), SPIRESIS (View Spiresis Review and Spiresis Label ), LYRICA (View Lyrica Review and Lyrica Label ). Patient was hospitalized.

6399896-6 | Blood Glucose Decreased, Hypoglycaemia, Incorrect Dose Administered, Overdose, Product Quality Issue
Patient was taking Apidra (View Usage). After Apidra was administered, patient had the following side effects: blood glucose decreased, hypoglycaemia, incorrect dose administered, overdose, product quality issue on Oct 08, 2009 from UNITED STATES Additional patient health information: Male patient , weighting 160.9 lb, . Apidra dosage: Dose: Unk. During the same period patient was treated with LANTUS (Dose: Unk) (View Lantus Review and Lantus Label ), OPTICLIK (INSULIN INJECTION PEN) (View Opticlik (insulin Injection Pen) Review and Opticlik (insulin Injection Pen) Label ).

6397028-1 | Acidosis, Hyperkalaemia, Pericardial Effusion, Pericarditis, Renal Failure Acute
Adverse event was reported on Jul 20, 2009 by a Male patient taking Apidra (View Usage) (Dosage: ) . Location: UNITED STATES , 71 years of age, weighting 178.4 lb, Patient experienced the following unwanted or unexpected effects: acidosis, hyperkalaemia, pericardial effusion, pericarditis, renal failure acute. During the same period patient was treated with LANTUS (View Lantus Review and Lantus Label ). Patient was hospitalized.

6395507-4 | Hyperbilirubinaemia, Metabolic Disorder, Premature Baby
on Oct 06, 2009 Female patient from SOUTH AFRICA , weighting 6.61 lb, was diagnosed with diabetic relative and was treated with Apidra (View Usage). Patient had the following side effects: hyperbilirubinaemia, metabolic disorder (What is metabolic disorder?), premature baby. Apidra dosage: . Patient was hospitalized.

6382464-X | Blood Glucose Increased, Liquid Product Physical Issue, Medical Device Complication
on Sep 28, 2009 Male patient from UNITED STATES , 45 years of age, was diagnosed with type 1 diabetes mellitus and was treated with Apidra (View Usage). After Apidra was administered, patient had the following side effects: blood glucose increased, liquid product physical issue, medical device complication. Apidra dosage: Use 100 Unts Continuously.

6380291-0 | Asthenia, Blood Glucose Increased, Confusional State, Costochondritis, Cushing's Syndrome, Dyspnoea, Epilepsy, Fall, Feeling Abnormal
Patient was taking Apidra (View Usage). Patient experienced the following unwanted or unexpected effects: asthenia, blood glucose increased, confusional state, costochondritis, cushing's syndrome, dyspnoea, epilepsy (What is epilepsy?), fall (What is fall?), feeling abnormal on Jun 13, 2009 from UNITED KINGDOM Additional patient health information: Female patient , weighting 232.0 lb, was diagnosed with cushing's syndrome, chest pain (What is chest pain?), asthma (What is asthma?), gastritis and. Apidra dosage: . During the same period patient was treated with LANTUS (View Lantus Review and Lantus Label ), ADCAL D3 (Dose Quantity: 1) (View Adcal D3 Review and Adcal D3 Label ), ALENDRONIC ACID (View Alendronic Acid Review and Alendronic Acid Label ), CLOPIDOGREL (View Clopidogrel Review and Clopidogrel Label ), SALBUTAMOL SULPHATE (View Salbutamol Sulphate Review and Salbutamol Sulphate Label ), LANSOPRAZOLE (View Lansoprazole Review and Lansoprazole Label ). Patient was hospitalized.

6354927-4 | Hyperbilirubinaemia, Metabolic Disorder, Premature Baby
Adverse event was reported on Sep 04, 2009 by a Female patient taking Apidra (View Usage) (Dosage: ) was diagnosed with diabetic relative and. Location: SOUTH AFRICA , weighting 6.61 lb, Patient had the following side effects: hyperbilirubinaemia, metabolic disorder (What is metabolic disorder?), premature baby. Patient was hospitalized.

6347864-2 | Hyperbilirubinaemia, Metabolic Disorder, Premature Baby
on Sep 02, 2009 Female patient from SOUTH AFRICA , weighting 6.61 lb, was diagnosed with diabetic relative and was treated with Apidra (View Usage). After Apidra was administered, patient had the following side effects: hyperbilirubinaemia, metabolic disorder (What is metabolic disorder?), premature baby. Apidra dosage: . Patient was hospitalized.

6334929-4 | Cerebrovascular Accident, Diabetes Mellitus Inadequate Control
on Aug 25, 2009 Female patient from UNITED STATES , weighting 183.0 lb, was treated with Apidra (View Usage). Patient experienced the following unwanted or unexpected effects: cerebrovascular accident, diabetes mellitus inadequate control. Apidra dosage: . During the same period patient was treated with OPTICLIK (INSULIN INJECTION PEN) (View Opticlik (insulin Injection Pen) Review and Opticlik (insulin Injection Pen) Label ), LANTUS (Dose: Unk) (View Lantus Review and Lantus Label ). Patient was hospitalized.

6334925-7 | Asthenia, Dyspnoea, Laryngeal Oedema
Patient was taking Apidra (View Usage). Patient had the following side effects: asthenia, dyspnoea, laryngeal oedema on Aug 25, 2009 from RUSSIAN FEDERATION Additional patient health information: Female patient , 54 years of age, weighting 216.1 lb, was diagnosed with diabetes mellitus and. Apidra dosage: . During the same period patient was treated with LANTUS (View Lantus Review and Lantus Label ).

6333114-X | Hyperbilirubinaemia, Metabolic Disorder, Premature Baby
Adverse event was reported on Aug 24, 2009 by a Female patient taking Apidra (View Usage) (Dosage: ) was diagnosed with diabetic relative and. Location: SOUTH AFRICA , weighting 6.61 lb, After Apidra was administered, patient had the following side effects: hyperbilirubinaemia, metabolic disorder (What is metabolic disorder?), premature baby. Patient was hospitalized.

6329367-4 | Asthenia, Dyspnoea, Laryngeal Oedema
on Aug 21, 2009 Female patient from RUSSIAN FEDERATION , 54 years of age, weighting 216.1 lb, was diagnosed with diabetes mellitus and was treated with Apidra (View Usage). Patient experienced the following unwanted or unexpected effects: asthenia, dyspnoea, laryngeal oedema. Apidra dosage: . During the same period patient was treated with LANTUS (View Lantus Review and Lantus Label ).

6327198-2 | Amnesia, Confusional State, Glycosylated Haemoglobin Increased, Hyperglycaemia, Hypoglycaemia, Hypoglycaemic Unconsciousness, Neck Injury, Road Traffic Accident
on Aug 14, 2009 Male patient from UNITED STATES , weighting 173.3 lb, was diagnosed with diabetes mellitus, blood pressure (What is blood pressure?), hypothyroidism and was treated with Apidra (View Usage). Patient had the following side effects: amnesia, confusional state, glycosylated haemoglobin increased, hyperglycaemia, hypoglycaemia, hypoglycaemic unconsciousness, neck injury, road traffic accident. Apidra dosage: Dose: 1-10 Units Sliding Scale Before Meals, Based On Premeal Blood Glucose. During the same period patient was treated with OPTICLIK (INSULIN INJECTION PEN) (View Opticlik (insulin Injection Pen) Review and Opticlik (insulin Injection Pen) Label ), LANTUS (View Lantus Review and Lantus Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), ISOSORBIDE MONONITRATE (View Isosorbide Mononitrate Review and Isosorbide Mononitrate Label ), LISINOPRIL (View Lisinopril Review and Lisinopril Label ), AMLODIPINE BESYLATE (View Amlodipine Besylate Review and Amlodipine Besylate Label ), HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ), LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ). Patient was hospitalized.

6315311-2 | Diabetic Ketoacidosis
Patient was taking Apidra (View Usage). After Apidra was administered, patient had the following side effects: diabetic ketoacidosis on Jun 10, 2009 from INDIA Additional patient health information: Female patient , 50 years of age, was diagnosed with diabetic ketoacidosis and. Apidra dosage: . Patient was hospitalized.

6308400-X | Eclampsia, Hypoglycaemia
Adverse event was reported on Aug 04, 2009 by a Female patient taking Apidra (View Usage) (Dosage: ) was diagnosed with hypothyroidism and. Location: FRANCE , 28 years of age, Patient experienced the following unwanted or unexpected effects: eclampsia, hypoglycaemia. During the same period patient was treated with ALDOMET /00000101/ (View Aldomet /00000101/ Review and Aldomet /00000101/ Label ), LEVOTHYROX (Dose: 67.5 To 150) (View Levothyrox Review and Levothyrox Label ).

6286708-4 | Cataract, Visual Impairment
on Jul 20, 2009 Male patient from UNITED STATES , weighting 195.3 lb, was treated with Apidra (View Usage). Patient had the following side effects: cataract (What is cataract?), visual impairment. Apidra dosage: . During the same period patient was treated with OPTICLIK GREY (View Opticlik Grey Review and Opticlik Grey Label ), TEARS NATURALE II (Dose: Unk) (View Tears Naturale Ii Review and Tears Naturale Ii Label ).

6284739-1 | Blood Glucose Increased
on Jul 16, 2009 Female patient from UNITED STATES , weighting 277.8 lb, was treated with Apidra (View Usage). After Apidra was administered, patient had the following side effects: blood glucose increased. Apidra dosage: Dose: 1-50 (sliding Scale) Depending On Carbs. During the same period patient was treated with OPTICLIK (INSULIN INJECTION PEN) (View Opticlik (insulin Injection Pen) Review and Opticlik (insulin Injection Pen) Label ), LANTUS (View Lantus Review and Lantus Label ), CYTOMEL (Dose: 1/2 Mcg) (View Cytomel Review and Cytomel Label ), NEXIUM (View Nexium Review and Nexium Label ), ADVAIR HFA (Dose: 500/50) (View Advair Hfa Review and Advair Hfa Label ), ALTACE (View Altace Review and Altace Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ), ASPIRIN (View Aspirin Review and Aspirin Label ).

6277928-3 | Acidosis, Hyperkalaemia, Pericarditis, Renal Failure Acute
Patient was taking Apidra (View Usage). Patient experienced the following unwanted or unexpected effects: acidosis, hyperkalaemia, pericarditis, renal failure acute on Jul 14, 2009 from UNITED STATES Additional patient health information: Male patient , 71 years of age, weighting 178.4 lb, . Apidra dosage: . During the same period patient was treated with LANTUS (View Lantus Review and Lantus Label ). Patient was hospitalized.

6267850-0 | Amnesia, Confusional State, Device Malfunction, Glycosylated Haemoglobin Increased, Hyperglycaemia, Hypoglycaemia, Hypoglycaemic Unconsciousness, Neck Injury, Road Traffic Accident
Adverse event was reported on Jul 06, 2009 by a Male patient taking Apidra (View Usage) (Dosage: Dose: 1-10 Units Sliding Scale Before Meals, Based On Premeal Blood Glucose) was diagnosed with diabetes mellitus, blood pressure (What is blood pressure?), hypothyroidism and. Location: UNITED STATES , weighting 173.3 lb, Patient had the following side effects: amnesia, confusional state, device malfunction, glycosylated haemoglobin increased, hyperglycaemia, hypoglycaemia, hypoglycaemic unconsciousness, neck injury, road traffic accident. During the same period patient was treated with OPTICLIK (INSULIN INJECTION PEN) (View Opticlik (insulin Injection Pen) Review and Opticlik (insulin Injection Pen) Label ), LANTUS (View Lantus Review and Lantus Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), ISOSORBIDE MONONITRATE (View Isosorbide Mononitrate Review and Isosorbide Mononitrate Label ), LISINOPRIL (View Lisinopril Review and Lisinopril Label ), AMLODIPINE BESYLATE (View Amlodipine Besylate Review and Amlodipine Besylate Label ), HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ), LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ). Patient was hospitalized.

6257638-9 | Amnesia, Blood Glucose Decreased, Cerebrovascular Accident
on Jun 29, 2009 Female patient from UNITED STATES , 53 years of age, was treated with Apidra (View Usage). After Apidra was administered, patient had the following side effects: amnesia, blood glucose decreased, cerebrovascular accident. Apidra dosage: Dose: Sliding Scale. During the same period patient was treated with OPTICLIK (INSULIN INJECTION PEN) (View Opticlik (insulin Injection Pen) Review and Opticlik (insulin Injection Pen) Label ), LANTUS (Dose: 14 Units Am And 22 Units In Pm) (View Lantus Review and Lantus Label ). Patient was hospitalized.

6254705-0 | Blood Glucose Increased, Ketosis, Overdose, Pain In Extremity
on Jun 24, 2009 Male patient from UNITED STATES , weighting 218.5 lb, was treated with Apidra (View Usage). Patient experienced the following unwanted or unexpected effects: blood glucose increased, ketosis, overdose, pain in extremity. Apidra dosage: Dose: Via Pump. During the same period patient was treated with MULTI VITAMINS (Dose: Unk) (View Multi-vitamins Review and Multi-vitamins Label ), ASCORBIC ACID (View Ascorbic Acid Review and Ascorbic Acid Label ), VIT D (View Vit D Review and Vit D Label ), CITRUCEL (Dose: Unk) (View Citrucel Review and Citrucel Label ), COMPAZINE (Dose: 10 Mg Three Times A Day Prn) (View Compazine Review and Compazine Label ), LORTAB (Dose: Unk) (View Lortab Review and Lortab Label ), SPIRIVA (Dose: Unk) (View Spiriva Review and Spiriva Label ).

6250622-0 | Blood Glucose Increased, Injection Site Haematoma
Patient was taking Apidra (View Usage). Patient had the following side effects: blood glucose increased, injection site haematoma on Jun 19, 2009 from UNITED STATES Additional patient health information: Male patient , 77 years of age, . Apidra dosage: Dose: Varies. During the same period patient was treated with OPTICLIK (INSULIN INJECTION PEN) (View Opticlik (insulin Injection Pen) Review and Opticlik (insulin Injection Pen) Label ).

6245324-0 | Injury Corneal, Retinal Detachment
Adverse event was reported on Jun 18, 2009 by a Male patient taking Apidra (View Usage) (Dosage: Dose: Sliding Scale) . Location: UNITED STATES , 61 years of age, After Apidra was administered, patient had the following side effects: injury corneal, retinal detachment. During the same period patient was treated with OPTICLIK GREY (View Opticlik Grey Review and Opticlik Grey Label ).

6240925-8 | Amnesia, Confusional State, Hyperglycaemia, Hypoglycaemia, Hypoglycaemic Unconsciousness, Neck Injury, Road Traffic Accident
on Jun 16, 2009 Male patient from UNITED STATES , weighting 179.4 lb, was diagnosed with diabetes mellitus and was treated with Apidra (View Usage). Patient experienced the following unwanted or unexpected effects: amnesia, confusional state, hyperglycaemia, hypoglycaemia, hypoglycaemic unconsciousness, neck injury, road traffic accident. Apidra dosage: Dose: 1-10 Units Sliding Scale Based On Premeal Blood Glucose. During the same period patient was treated with OPTICLIK (INSULIN INJECTION PEN) (View Opticlik (insulin Injection Pen) Review and Opticlik (insulin Injection Pen) Label ), LANTUS (View Lantus Review and Lantus Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), ISOSORBIDE MONONITRATE (View Isosorbide Mononitrate Review and Isosorbide Mononitrate Label ), LISINOPRIL (View Lisinopril Review and Lisinopril Label ), AMLODIPINE BESYLATE (View Amlodipine Besylate Review and Amlodipine Besylate Label ), HYDROCHLOROTHIAZDE TAB (View Hydrochlorothiazde Tab Review and Hydrochlorothiazde Tab Label ), LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ). Patient was hospitalized.

6229984-6 | Blood Glucose Increased, Organising Pneumonia
on Jun 09, 2009 Female patient from UNITED STATES , 64 years of age, was treated with Apidra (View Usage). Patient had the following side effects: blood glucose increased, organising pneumonia. Apidra dosage: Dose: 1-50 (sliding Scale) Depending On Carbs. During the same period patient was treated with OPTICLIK (INSULIN INJECTION PEN) (View Opticlik (insulin Injection Pen) Review and Opticlik (insulin Injection Pen) Label ), LANTUS (View Lantus Review and Lantus Label ).

6204313-2 | Hyperbilirubinaemia, Metabolic Disorder, Premature Baby
Patient was taking Apidra (View Usage). After Apidra was administered, patient had the following side effects: hyperbilirubinaemia, metabolic disorder (What is metabolic disorder?), premature baby on May 20, 2009 from SOUTH AFRICA Additional patient health information: Female patient , weighting 6.61 lb, was diagnosed with diabetic relative and. Apidra dosage: . Patient was hospitalized.

6202118-X | Cardiac Disorder, Skin Discolouration, Skin Ulcer
Adverse event was reported on May 17, 2009 by a Male patient taking Apidra (View Usage) (Dosage: Dose: 5 Units) . Location: UNITED STATES , 73 years of age, Patient experienced the following unwanted or unexpected effects: cardiac disorder, skin discolouration, skin ulcer. During the same period patient was treated with OPTICLIK GREY (Dose: Unk) (View Opticlik Grey Review and Opticlik Grey Label ), LANTUS (Dose: Unk) (View Lantus Review and Lantus Label ).

6198239-0 | Blood Glucose Increased, Injection Site Haematoma
on May 08, 2009 Male patient from UNITED STATES , 77 years of age, was treated with Apidra (View Usage). Patient had the following side effects: blood glucose increased, injection site haematoma. Apidra dosage: Dose: Varies. During the same period patient was treated with OPTICLIK (INSULIN INJECTION PEN) (View Opticlik (insulin Injection Pen) Review and Opticlik (insulin Injection Pen) Label ).

6196204-0 | Diabetic Ketoacidosis, Product Quality Issue
on May 07, 2009 Female patient from SOUTH AFRICA , child 11 years of age, was treated with Apidra (View Usage). After Apidra was administered, patient had the following side effects: diabetic ketoacidosis, product quality issue. Apidra dosage: . During the same period patient was treated with INSULIN PUMP NOS (View Insulin Pump Nos Review and Insulin Pump Nos Label ). Patient was hospitalized.

6194930-0 | Chest Pain, Dizziness, Epistaxis, Hyperhidrosis
Patient was taking Apidra (View Usage). Patient experienced the following unwanted or unexpected effects: chest pain (What is chest pain?), dizziness (What is dizziness?), epistaxis, hyperhidrosis on May 08, 2009 from INDIA Additional patient health information: Male patient , 62 years of age, was diagnosed with diabetes mellitus and. Apidra dosage: . During the same period patient was treated with TAXOTERE (View Taxotere Review and Taxotere Label ), CORTICOSTEROIDS (View Corticosteroids Review and Corticosteroids Label ), ANTIHISTAMINES (View Antihistamines Review and Antihistamines Label ). Patient was hospitalized.

6194928-2 | Hyperbilirubinaemia, Metabolic Disorder, Premature Baby
Adverse event was reported on May 08, 2009 by a Female patient taking Apidra (View Usage) (Dosage: ) was diagnosed with diabetic relative and. Location: SOUTH AFRICA , weighting 6.61 lb, Patient had the following side effects: hyperbilirubinaemia, metabolic disorder (What is metabolic disorder?), premature baby. Patient was hospitalized.

6186147-0 | Angina Pectoris, Dizziness, Epistaxis, Hyperhidrosis
on May 06, 2009 Male patient from INDIA , 62 years of age, was diagnosed with diabetes mellitus and was treated with Apidra (View Usage). After Apidra was administered, patient had the following side effects: angina pectoris, dizziness (What is dizziness?), epistaxis, hyperhidrosis. Apidra dosage: . Patient was hospitalized.

6180518-4 | Hypoglycaemia, Incorrect Dose Administered, Product Outer Packaging Issue, Product Quality Issue
on May 04, 2009 Female patient from UNITED STATES , 31 years of age, was diagnosed with type 1 diabetes mellitus and was treated with Apidra (View Usage). Patient experienced the following unwanted or unexpected effects: hypoglycaemia, incorrect dose administered, product outer packaging issue, product quality issue. Apidra dosage: 4-8 Units With Meals Bid Sq. During the same period patient was treated with LANTUS (25 Units Qam Sq) (View Lantus Review and Lantus Label ).

6179593-2 | Blood Glucose Increased, Ketosis, Overdose, Pain In Extremity
Patient was taking Apidra (View Usage). Patient had the following side effects: blood glucose increased, ketosis, overdose, pain in extremity on Apr 27, 2009 from UNITED STATES Additional patient health information: Male patient , weighting 218.5 lb, . Apidra dosage: Dose: Via Pump. During the same period patient was treated with MULTI VITAMINS (Dose: Unk) (View Multi-vitamins Review and Multi-vitamins Label ), ASCORBIC ACID (View Ascorbic Acid Review and Ascorbic Acid Label ), VIT D (View Vit D Review and Vit D Label ), CITRUCEL (Dose: Unk) (View Citrucel Review and Citrucel Label ), COMPAZINE (Dose: 10 Mg Three Times A Day Prn) (View Compazine Review and Compazine Label ), LORTAB (Dose: Unk) (View Lortab Review and Lortab Label ), SPIRIVA (Dose: Unk) (View Spiriva Review and Spiriva Label ).