Please choose an event type to view the corresponding MedsFacts report:

WEIGHT INCREASED ( 9 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 8 FDA reports)
PRESCRIBED OVERDOSE ( 8 FDA reports)
CONSTIPATION ( 7 FDA reports)
DIABETES MELLITUS ( 7 FDA reports)
PSYCHOTIC DISORDER ( 7 FDA reports)
BLOOD GLUCOSE INCREASED ( 6 FDA reports)
ASTHENIA ( 5 FDA reports)
BIPOLAR DISORDER ( 5 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 5 FDA reports)
HIATUS HERNIA ( 5 FDA reports)
LOSS OF CONSCIOUSNESS ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
CARDIO-RESPIRATORY ARREST ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
RESPIRATORY ARREST ( 4 FDA reports)
STOMACH DISCOMFORT ( 4 FDA reports)
HAEMATOCRIT DECREASED ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HALLUCINATION ( 3 FDA reports)
INCONTINENCE ( 3 FDA reports)
INJECTION SITE REACTION ( 3 FDA reports)
MANIA ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
FACIAL PALSY ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ANKLE FRACTURE ( 1 FDA reports)
ANOXIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CATARACT OPERATION ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
FAECES HARD ( 1 FDA reports)
FALL ( 1 FDA reports)
FOOT FRACTURE ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOMANIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
INJECTION SITE HYPERTROPHY ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
JOINT SPRAIN ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LEUKAEMIA ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL SURGERY ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
THERMAL BURN ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
ULCER ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
VOMITING ( 1 FDA reports)

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