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

NAUSEA ( 18 FDA reports)
DIARRHOEA ( 16 FDA reports)
FALL ( 13 FDA reports)
DRUG INEFFECTIVE ( 12 FDA reports)
HEADACHE ( 11 FDA reports)
TREMOR ( 10 FDA reports)
COUGH ( 9 FDA reports)
GASTROINTESTINAL DISORDER ( 9 FDA reports)
DYSGEUSIA ( 8 FDA reports)
FATIGUE ( 8 FDA reports)
FEELING ABNORMAL ( 8 FDA reports)
FLATULENCE ( 8 FDA reports)
HOT FLUSH ( 8 FDA reports)
HYPERTENSION ( 8 FDA reports)
HYPOTENSION ( 8 FDA reports)
ILL-DEFINED DISORDER ( 8 FDA reports)
INTENTIONAL DRUG MISUSE ( 8 FDA reports)
MYOCARDIAL ISCHAEMIA ( 8 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 8 FDA reports)
ABNORMAL FAECES ( 7 FDA reports)
ACCIDENT ( 7 FDA reports)
ADVERSE EVENT ( 7 FDA reports)
ASTHENIA ( 7 FDA reports)
DEFAECATION URGENCY ( 7 FDA reports)
EPISTAXIS ( 7 FDA reports)
FOOD CRAVING ( 7 FDA reports)
HIP FRACTURE ( 7 FDA reports)
HORMONE LEVEL ABNORMAL ( 7 FDA reports)
HUNGER ( 7 FDA reports)
LIMB INJURY ( 7 FDA reports)
MEDICATION ERROR ( 7 FDA reports)
NASOPHARYNGITIS ( 7 FDA reports)
OEDEMA PERIPHERAL ( 7 FDA reports)
WEIGHT FLUCTUATION ( 7 FDA reports)
WEIGHT INCREASED ( 7 FDA reports)
DYSPNOEA ( 6 FDA reports)
HAEMODIALYSIS ( 6 FDA reports)
LACTIC ACIDOSIS ( 6 FDA reports)
MALAISE ( 6 FDA reports)
PRODUCT QUALITY ISSUE ( 6 FDA reports)
RENAL FAILURE ACUTE ( 6 FDA reports)
VOMITING ( 6 FDA reports)
AGITATION ( 5 FDA reports)
APACHE II SCORE ( 5 FDA reports)
BLADDER CANCER ( 5 FDA reports)
BURNING SENSATION ( 5 FDA reports)
GAIT DISTURBANCE ( 5 FDA reports)
HYPERKERATOSIS ( 5 FDA reports)
INFLUENZA LIKE ILLNESS ( 5 FDA reports)
NERVE COMPRESSION ( 5 FDA reports)
RASH ( 5 FDA reports)
SENSORY LOSS ( 5 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 5 FDA reports)
WEIGHT DECREASED ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 4 FDA reports)
CORONARY ARTERY DISEASE ( 4 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 4 FDA reports)
INGUINAL HERNIA ( 4 FDA reports)
MYOCARDIAL INFARCTION ( 4 FDA reports)
PALPITATIONS ( 4 FDA reports)
ABDOMINAL DISTENSION ( 3 FDA reports)
ANGER ( 3 FDA reports)
ANGINA PECTORIS ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
CUTANEOUS LEISHMANIASIS ( 3 FDA reports)
DERMATITIS EXFOLIATIVE ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 3 FDA reports)
HAEMATURIA ( 3 FDA reports)
LIVER INJURY ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
MITRAL VALVE INCOMPETENCE ( 3 FDA reports)
MOOD SWINGS ( 3 FDA reports)
MUSCULAR WEAKNESS ( 3 FDA reports)
NON-SMALL CELL LUNG CANCER ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
SLEEP DISORDER ( 3 FDA reports)
SWELLING ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
ABDOMINAL CAVITY DRAINAGE ( 2 FDA reports)
ANEURYSM ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BONE NEOPLASM ( 2 FDA reports)
CARDIAC VALVE DISEASE ( 2 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DISTURBANCE IN ATTENTION ( 2 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 2 FDA reports)
DRUG ADMINISTRATION ERROR ( 2 FDA reports)
DRUG DOSE OMISSION ( 2 FDA reports)
EYE SWELLING ( 2 FDA reports)
FEAR ( 2 FDA reports)
FIBROMYALGIA ( 2 FDA reports)
GASTRIC BYPASS ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
HYPERPHAGIA ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
INCISION SITE INFECTION ( 2 FDA reports)
INCOHERENT ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
ORAL PAIN ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
PITTING OEDEMA ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
TEARFULNESS ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
TRACHEOSTOMY ( 2 FDA reports)
VENTRICULAR ARRHYTHMIA ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
WOUND DEHISCENCE ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
ADVERSE REACTION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANEURYSM RUPTURED ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHAPPED LIPS ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHLOROPSIA ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEPENDENCE ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GINGIVAL SWELLING ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
INFECTION ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LISTLESS ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
METASTASES TO SOFT TISSUE ( 1 FDA reports)
METASTASES TO SPLEEN ( 1 FDA reports)
MUSCLE STRAIN ( 1 FDA reports)
NASAL SINUS CANCER ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAINFUL RESPIRATION ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PERFORATED ULCER ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
POLYP ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RECTAL DISCHARGE ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
RENAL HAEMORRHAGE ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SKIN CANCER ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SOFT TISSUE INFECTION ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)

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