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

DRUG INEFFECTIVE ( 77 FDA reports)
NAUSEA ( 75 FDA reports)
HEADACHE ( 49 FDA reports)
PAIN ( 42 FDA reports)
FATIGUE ( 41 FDA reports)
VOMITING ( 40 FDA reports)
CHEST PAIN ( 38 FDA reports)
DEPRESSION ( 38 FDA reports)
MIGRAINE ( 37 FDA reports)
ANXIETY ( 36 FDA reports)
ARTHRALGIA ( 34 FDA reports)
DIZZINESS ( 31 FDA reports)
ASTHENIA ( 29 FDA reports)
ABDOMINAL PAIN UPPER ( 26 FDA reports)
CONVULSION ( 26 FDA reports)
DYSPNOEA ( 26 FDA reports)
INSOMNIA ( 26 FDA reports)
HYPOAESTHESIA ( 25 FDA reports)
DIARRHOEA ( 23 FDA reports)
PYREXIA ( 23 FDA reports)
TREMOR ( 23 FDA reports)
PAIN IN EXTREMITY ( 22 FDA reports)
PULMONARY EMBOLISM ( 22 FDA reports)
DRUG DEPENDENCE ( 20 FDA reports)
LOSS OF CONSCIOUSNESS ( 20 FDA reports)
MALAISE ( 19 FDA reports)
PARAESTHESIA ( 19 FDA reports)
PHOTOPHOBIA ( 19 FDA reports)
CONFUSIONAL STATE ( 18 FDA reports)
WEIGHT DECREASED ( 18 FDA reports)
ALOPECIA ( 17 FDA reports)
BACK PAIN ( 17 FDA reports)
INJURY ( 17 FDA reports)
NECK PAIN ( 17 FDA reports)
CHILLS ( 16 FDA reports)
CONDITION AGGRAVATED ( 16 FDA reports)
DISTURBANCE IN ATTENTION ( 16 FDA reports)
TINNITUS ( 16 FDA reports)
ANOREXIA ( 15 FDA reports)
BALANCE DISORDER ( 15 FDA reports)
HYPERHIDROSIS ( 15 FDA reports)
RASH ( 15 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 14 FDA reports)
ABDOMINAL DISTENSION ( 13 FDA reports)
CHEST DISCOMFORT ( 13 FDA reports)
CRYING ( 13 FDA reports)
FEELING ABNORMAL ( 13 FDA reports)
MENORRHAGIA ( 13 FDA reports)
MUSCLE SPASMS ( 13 FDA reports)
PALPITATIONS ( 13 FDA reports)
PETECHIAE ( 13 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 13 FDA reports)
SALIVARY HYPERSECRETION ( 13 FDA reports)
SOMNOLENCE ( 13 FDA reports)
VIRAL INFECTION ( 13 FDA reports)
VISION BLURRED ( 13 FDA reports)
CONSTIPATION ( 12 FDA reports)
FALL ( 12 FDA reports)
INADEQUATE ANALGESIA ( 12 FDA reports)
MEMORY IMPAIRMENT ( 12 FDA reports)
MYOCARDIAL INFARCTION ( 12 FDA reports)
SUICIDAL IDEATION ( 12 FDA reports)
DEEP VEIN THROMBOSIS ( 11 FDA reports)
DYSARTHRIA ( 11 FDA reports)
EYE PAIN ( 11 FDA reports)
GALLBLADDER DISORDER ( 11 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 11 FDA reports)
SPEECH DISORDER ( 11 FDA reports)
SYNCOPE ( 11 FDA reports)
ABDOMINAL PAIN ( 10 FDA reports)
ABNORMAL BEHAVIOUR ( 10 FDA reports)
AMNESIA ( 10 FDA reports)
BLOOD PRESSURE INCREASED ( 10 FDA reports)
CHOLECYSTITIS CHRONIC ( 10 FDA reports)
DRUG TOLERANCE ( 10 FDA reports)
EAR PAIN ( 10 FDA reports)
EMOTIONAL DISTRESS ( 10 FDA reports)
HAEMOGLOBIN DECREASED ( 10 FDA reports)
HYSTERECTOMY ( 10 FDA reports)
NEPHROLITHIASIS ( 10 FDA reports)
NERVOUSNESS ( 10 FDA reports)
WEIGHT INCREASED ( 10 FDA reports)
CYSTITIS ( 9 FDA reports)
DEAFNESS ( 9 FDA reports)
DIPLOPIA ( 9 FDA reports)
DRUG ABUSER ( 9 FDA reports)
DRUG TOXICITY ( 9 FDA reports)
ERYTHEMA ( 9 FDA reports)
EUPHORIC MOOD ( 9 FDA reports)
HAEMATURIA ( 9 FDA reports)
HAIR PLUCKING ( 9 FDA reports)
HEART RATE INCREASED ( 9 FDA reports)
IRRITABILITY ( 9 FDA reports)
OVERDOSE ( 9 FDA reports)
RENAL PAIN ( 9 FDA reports)
TONGUE DISORDER ( 9 FDA reports)
URINARY RETENTION ( 9 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 8 FDA reports)
DYSSTASIA ( 8 FDA reports)
EPISTAXIS ( 8 FDA reports)
FACIAL PAIN ( 8 FDA reports)
FAECAL INCONTINENCE ( 8 FDA reports)
HALLUCINATION ( 8 FDA reports)
HALLUCINATION, VISUAL ( 8 FDA reports)
HYPERTENSION ( 8 FDA reports)
IMPAIRED HEALING ( 8 FDA reports)
INFLUENZA LIKE ILLNESS ( 8 FDA reports)
LACRIMATION INCREASED ( 8 FDA reports)
MENTAL DISORDER ( 8 FDA reports)
MENTAL STATUS CHANGES ( 8 FDA reports)
PARONYCHIA ( 8 FDA reports)
PHARYNGITIS ( 8 FDA reports)
PRODUCT QUALITY ISSUE ( 8 FDA reports)
RHINORRHOEA ( 8 FDA reports)
SEDATION ( 8 FDA reports)
STRESS ( 8 FDA reports)
TACHYCARDIA ( 8 FDA reports)
WOUND DEHISCENCE ( 8 FDA reports)
YAWNING ( 8 FDA reports)
ABDOMINAL PAIN LOWER ( 7 FDA reports)
CEREBROVASCULAR ACCIDENT ( 7 FDA reports)
CHANGE OF BOWEL HABIT ( 7 FDA reports)
COLITIS ISCHAEMIC ( 7 FDA reports)
COMPLEX PARTIAL SEIZURES ( 7 FDA reports)
DEHYDRATION ( 7 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 7 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 7 FDA reports)
DRY SKIN ( 7 FDA reports)
DYSPAREUNIA ( 7 FDA reports)
DYSURIA ( 7 FDA reports)
HEPATIC ENZYME INCREASED ( 7 FDA reports)
MALNUTRITION ( 7 FDA reports)
MUSCLE CRAMP ( 7 FDA reports)
MYALGIA ( 7 FDA reports)
OVARIAN CYST ( 7 FDA reports)
PELVIC PAIN ( 7 FDA reports)
POSTOPERATIVE ADHESION ( 7 FDA reports)
PRURITUS ( 7 FDA reports)
ROAD TRAFFIC ACCIDENT ( 7 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 7 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 7 FDA reports)
URINARY TRACT INFECTION ( 7 FDA reports)
VASOSPASM ( 7 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 7 FDA reports)
ANGINA PECTORIS ( 6 FDA reports)
ARTERIOSPASM CORONARY ( 6 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 6 FDA reports)
CARDIOMYOPATHY ( 6 FDA reports)
DRUG INTERACTION ( 6 FDA reports)
ENDOCARDITIS ( 6 FDA reports)
FLUSHING ( 6 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 6 FDA reports)
INJECTION SITE HAEMORRHAGE ( 6 FDA reports)
LACERATION ( 6 FDA reports)
MICTURITION URGENCY ( 6 FDA reports)
OEDEMA PERIPHERAL ( 6 FDA reports)
OTITIS MEDIA ( 6 FDA reports)
PLATELET COUNT DECREASED ( 6 FDA reports)
POLYCYSTIC LIVER DISEASE ( 6 FDA reports)
RECTAL HAEMORRHAGE ( 6 FDA reports)
RENAL FAILURE ACUTE ( 6 FDA reports)
SLEEP DISORDER ( 6 FDA reports)
THINKING ABNORMAL ( 6 FDA reports)
ABORTION SPONTANEOUS ( 5 FDA reports)
ACCIDENTAL OVERDOSE ( 5 FDA reports)
AGITATION ( 5 FDA reports)
ANGER ( 5 FDA reports)
ATELECTASIS ( 5 FDA reports)
BONE PAIN ( 5 FDA reports)
BRONCHITIS ( 5 FDA reports)
CATARACT ( 5 FDA reports)
CHOLELITHIASIS ( 5 FDA reports)
COORDINATION ABNORMAL ( 5 FDA reports)
COUGH ( 5 FDA reports)
DEFAECATION URGENCY ( 5 FDA reports)
ELECTROCUTION ( 5 FDA reports)
ERECTILE DYSFUNCTION ( 5 FDA reports)
GALLBLADDER OPERATION ( 5 FDA reports)
GRAND MAL CONVULSION ( 5 FDA reports)
HALLUCINATIONS, MIXED ( 5 FDA reports)
INNER EAR DISORDER ( 5 FDA reports)
LYMPH NODE CALCIFICATION ( 5 FDA reports)
MENTAL IMPAIRMENT ( 5 FDA reports)
MULTIPLE DRUG OVERDOSE ( 5 FDA reports)
MUSCULAR WEAKNESS ( 5 FDA reports)
NEUROPATHY PERIPHERAL ( 5 FDA reports)
NEUTROPENIA ( 5 FDA reports)
NIGHTMARE ( 5 FDA reports)
ORAL FUNGAL INFECTION ( 5 FDA reports)
PAIN IN JAW ( 5 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 5 FDA reports)
SKIN LESION ( 5 FDA reports)
STOMACH DISCOMFORT ( 5 FDA reports)
SWOLLEN TONGUE ( 5 FDA reports)
URTICARIA ( 5 FDA reports)
WHEEZING ( 5 FDA reports)
ABDOMINAL ADHESIONS ( 4 FDA reports)
ABDOMINAL TENDERNESS ( 4 FDA reports)
ACCIDENT AT WORK ( 4 FDA reports)
ACUTE CORONARY SYNDROME ( 4 FDA reports)
ANAEMIA ( 4 FDA reports)
ARTHRITIS BACTERIAL ( 4 FDA reports)
BILIARY DYSKINESIA ( 4 FDA reports)
BIPOLAR DISORDER ( 4 FDA reports)
BLOOD BILIRUBIN INCREASED ( 4 FDA reports)
BLOOD POTASSIUM DECREASED ( 4 FDA reports)
CELLULITIS ( 4 FDA reports)
CEREBRAL INFARCTION ( 4 FDA reports)
CHROMATURIA ( 4 FDA reports)
DERMATITIS CONTACT ( 4 FDA reports)
DILATATION ATRIAL ( 4 FDA reports)
DISCOMFORT ( 4 FDA reports)
DISEASE RECURRENCE ( 4 FDA reports)
DRUG EFFECT DECREASED ( 4 FDA reports)
DRY MOUTH ( 4 FDA reports)
DYSGEUSIA ( 4 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 4 FDA reports)
EMBOLIC STROKE ( 4 FDA reports)
FEELING HOT ( 4 FDA reports)
FLANK PAIN ( 4 FDA reports)
FOOD INTOLERANCE ( 4 FDA reports)
HAEMATOCRIT DECREASED ( 4 FDA reports)
HEAD INJURY ( 4 FDA reports)
HEART RATE IRREGULAR ( 4 FDA reports)
HEPATIC STEATOSIS ( 4 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 4 FDA reports)
INJECTION SITE PAIN ( 4 FDA reports)
JAW DISORDER ( 4 FDA reports)
JOINT EFFUSION ( 4 FDA reports)
MITRAL VALVE INCOMPETENCE ( 4 FDA reports)
MOOD SWINGS ( 4 FDA reports)
MOTOR DYSFUNCTION ( 4 FDA reports)
MOVEMENT DISORDER ( 4 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 4 FDA reports)
MUSCLE TWITCHING ( 4 FDA reports)
MYOCARDIAL ISCHAEMIA ( 4 FDA reports)
NASOPHARYNGEAL DISORDER ( 4 FDA reports)
OESOPHAGEAL DISORDER ( 4 FDA reports)
PLEURITIC PAIN ( 4 FDA reports)
RESTLESSNESS ( 4 FDA reports)
RHINITIS ( 4 FDA reports)
SEPSIS ( 4 FDA reports)
SEROTONIN SYNDROME ( 4 FDA reports)
SPINAL FUSION SURGERY ( 4 FDA reports)
STAPHYLOCOCCAL INFECTION ( 4 FDA reports)
STRESS CARDIOMYOPATHY ( 4 FDA reports)
THROMBOCYTOPENIA ( 4 FDA reports)
TONGUE HAEMORRHAGE ( 4 FDA reports)
VISUAL FIELD DEFECT ( 4 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 4 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 4 FDA reports)
ABDOMINAL DISCOMFORT ( 3 FDA reports)
ACCIDENT ( 3 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 3 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 3 FDA reports)
ACUTE SINUSITIS ( 3 FDA reports)
ANHEDONIA ( 3 FDA reports)
ANXIETY DISORDER ( 3 FDA reports)
APHAGIA ( 3 FDA reports)
APHASIA ( 3 FDA reports)
ASTHMA ( 3 FDA reports)
ATRIAL SEPTAL DEFECT ( 3 FDA reports)
BILIARY ADENOMA ( 3 FDA reports)
BLOOD PRESSURE DECREASED ( 3 FDA reports)
BREAST FIBROMA ( 3 FDA reports)
BREAST PAIN ( 3 FDA reports)
BRUXISM ( 3 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 3 FDA reports)
CARDIAC VALVE VEGETATION ( 3 FDA reports)
CEREBROVASCULAR DISORDER ( 3 FDA reports)
CHOLECYSTITIS ( 3 FDA reports)
CONCUSSION ( 3 FDA reports)
CORONARY ARTERY DISEASE ( 3 FDA reports)
CYST ( 3 FDA reports)
DEATH ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
DEMYELINATION ( 3 FDA reports)
DIABETES MELLITUS ( 3 FDA reports)
DRUG DOSE OMISSION ( 3 FDA reports)
DRUG SCREEN POSITIVE ( 3 FDA reports)
DYSKINESIA ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
EYELID PTOSIS ( 3 FDA reports)
FEAR ( 3 FDA reports)
GAS POISONING ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
HALLUCINATION, AUDITORY ( 3 FDA reports)
HEPATIC ADENOMA ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
HYPERSOMNIA ( 3 FDA reports)
HYPOAESTHESIA ORAL ( 3 FDA reports)
IMPAIRED DRIVING ABILITY ( 3 FDA reports)
INCREASED TENDENCY TO BRUISE ( 3 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 3 FDA reports)
INFUSION RELATED REACTION ( 3 FDA reports)
INJECTION SITE ERYTHEMA ( 3 FDA reports)
IRON DEFICIENCY ANAEMIA ( 3 FDA reports)
JOINT STIFFNESS ( 3 FDA reports)
MEDICATION ERROR ( 3 FDA reports)
MIOSIS ( 3 FDA reports)
MOBILITY DECREASED ( 3 FDA reports)
MUSCLE TIGHTNESS ( 3 FDA reports)
MUSCULOSKELETAL PAIN ( 3 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 3 FDA reports)
NERVOUS SYSTEM DISORDER ( 3 FDA reports)
NEUTROPHIL COUNT DECREASED ( 3 FDA reports)
OFF LABEL USE ( 3 FDA reports)
OSTEOPENIA ( 3 FDA reports)
PARALYSIS ( 3 FDA reports)
PRESCRIBED OVERDOSE ( 3 FDA reports)
PULMONARY CONGESTION ( 3 FDA reports)
PULMONARY THROMBOSIS ( 3 FDA reports)
REVERSIBLE AIRWAYS OBSTRUCTION ( 3 FDA reports)
SENSATION OF FOREIGN BODY ( 3 FDA reports)
SHOULDER PAIN ( 3 FDA reports)
SINUSITIS ( 3 FDA reports)
SKIN DISCOLOURATION ( 3 FDA reports)
SKIN REACTION ( 3 FDA reports)
SWELLING ( 3 FDA reports)
TENDERNESS ( 3 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 3 FDA reports)
THROMBOSIS ( 3 FDA reports)
TOOTH DISORDER ( 3 FDA reports)
TROPONIN T ( 3 FDA reports)
TROPONIN T INCREASED ( 3 FDA reports)
TYPE 2 DIABETES MELLITUS ( 3 FDA reports)
VISUAL DISTURBANCE ( 3 FDA reports)
ABORTION ( 2 FDA reports)
ABSCESS ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
ANOSMIA ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BILIRUBINURIA ( 2 FDA reports)
BIPOLAR I DISORDER ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
BONE GRAFT ( 2 FDA reports)
BREAST CANCER IN SITU ( 2 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CARDIAC FLUTTER ( 2 FDA reports)
CEREBRAL CALCIFICATION ( 2 FDA reports)
CLOSTRIDIAL INFECTION ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 2 FDA reports)
CONGENITAL CYSTIC DISEASE OF LIVER ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
COOMBS TEST POSITIVE ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
DIZZINESS POSTURAL ( 2 FDA reports)
DRUG ABUSE ( 2 FDA reports)
DRUG ADMINISTRATION ERROR ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
DYSTONIA ( 2 FDA reports)
EAR DISCOMFORT ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
ENDOMETRIOSIS ( 2 FDA reports)
EXERCISE TOLERANCE DECREASED ( 2 FDA reports)
EXOSTOSIS ( 2 FDA reports)
EXPIRED DRUG ADMINISTERED ( 2 FDA reports)
EXPOSURE TO TOXIC AGENT ( 2 FDA reports)
EYE SWELLING ( 2 FDA reports)
FACIAL PALSY ( 2 FDA reports)
FOOD CRAVING ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
GASTROINTESTINAL NECROSIS ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HEART INJURY ( 2 FDA reports)
HEMIPLEGIA ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HIATUS HERNIA ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HYPERLIPIDAEMIA ( 2 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
INCONTINENCE ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
INJECTION SITE HAEMATOMA ( 2 FDA reports)
INJECTION SITE REACTION ( 2 FDA reports)
INTENTIONAL DRUG MISUSE ( 2 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 2 FDA reports)
INTESTINAL ISCHAEMIA ( 2 FDA reports)
IRRITABLE BOWEL SYNDROME ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
LARGE INTESTINAL ULCER ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
LEUKOENCEPHALOPATHY ( 2 FDA reports)
LIBIDO DECREASED ( 2 FDA reports)
LIMB INJURY ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
LUMBAR RADICULOPATHY ( 2 FDA reports)
LUNG CONSOLIDATION ( 2 FDA reports)
LUNG INFECTION ( 2 FDA reports)
MAJOR DEPRESSION ( 2 FDA reports)
MANIA ( 2 FDA reports)
MENISCUS LESION ( 2 FDA reports)
MITRAL VALVE DISEASE ( 2 FDA reports)
MUSCLE ATROPHY ( 2 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 2 FDA reports)
MUSCLE RIGIDITY ( 2 FDA reports)
MUSCLE STRAIN ( 2 FDA reports)
NEUROPATHY ( 2 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 2 FDA reports)
NONSPECIFIC REACTION ( 2 FDA reports)
ORAL CANDIDIASIS ( 2 FDA reports)
ORAL PAIN ( 2 FDA reports)
OROPHARYNGEAL PAIN ( 2 FDA reports)
OTITIS MEDIA ACUTE ( 2 FDA reports)
PAPILLOMA VIRAL INFECTION ( 2 FDA reports)
PATHOLOGICAL GAMBLING ( 2 FDA reports)
POLYSUBSTANCE ABUSE ( 2 FDA reports)
PRESYNCOPE ( 2 FDA reports)
PSYCHOTIC DISORDER ( 2 FDA reports)
RASH MACULAR ( 2 FDA reports)
REFLEX SYMPATHETIC DYSTROPHY ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
RESPIRATORY RATE INCREASED ( 2 FDA reports)
RESPIRATORY TRACT CONGESTION ( 2 FDA reports)
RETINAL DETACHMENT ( 2 FDA reports)
SCAN WITH CONTRAST ( 2 FDA reports)
SCAR ( 2 FDA reports)
SENSATION OF PRESSURE ( 2 FDA reports)
SINUS DISORDER ( 2 FDA reports)
SINUS HEADACHE ( 2 FDA reports)
SKIN INFECTION ( 2 FDA reports)
SNORING ( 2 FDA reports)
SPINAL OSTEOARTHRITIS ( 2 FDA reports)
SPLENOMEGALY ( 2 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
TARDIVE DYSKINESIA ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
THROAT TIGHTNESS ( 2 FDA reports)
TONGUE DISCOLOURATION ( 2 FDA reports)
TONGUE INJURY ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
UNRESPONSIVE TO STIMULI ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
VITAMIN B12 INCREASED ( 2 FDA reports)
WOUND ( 2 FDA reports)
WOUND DRAINAGE ( 2 FDA reports)
WOUND SECRETION ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABNORMAL CLOTTING FACTOR ( 1 FDA reports)
ACCIDENTAL DEATH ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACCIDENTAL POISONING ( 1 FDA reports)
ACNE ( 1 FDA reports)
ADHESIOLYSIS ( 1 FDA reports)
ADHESION ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
AGORAPHOBIA ( 1 FDA reports)
ALCOHOL ABUSE ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ALCOHOLISM ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
AMENORRHOEA ( 1 FDA reports)
ANALGESIC DRUG LEVEL DECREASED ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANORECTAL DISCOMFORT ( 1 FDA reports)
ANORECTAL DISORDER ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES ( 1 FDA reports)
APPLICATION SITE ERYTHEMA ( 1 FDA reports)
APPLICATION SITE PAIN ( 1 FDA reports)
APPLICATION SITE PRURITUS ( 1 FDA reports)
APPLICATION SITE RASH ( 1 FDA reports)
APPLICATION SITE VESICLES ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ARTHROPOD STING ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ATROPHY ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BACTERIAL SEPSIS ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BONE DENSITY ABNORMAL ( 1 FDA reports)
BRAIN DAMAGE ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
BREAST DISORDER ( 1 FDA reports)
BREAST TENDERNESS ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
BURSITIS ( 1 FDA reports)
CALCULUS URETHRAL ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 1 FDA reports)
CENTRAL PAIN SYNDROME ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
CEREBRAL PALSY ( 1 FDA reports)
CERVICAL DYSPLASIA ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHONDROMALACIA ( 1 FDA reports)
CHOREA ( 1 FDA reports)
CHRONIC HEPATITIS ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
CLUMSINESS ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
COMPARTMENT SYNDROME ( 1 FDA reports)
CONGENITAL ANOMALY ( 1 FDA reports)
CONGENITAL ATRIAL SEPTAL DEFECT ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
CSF VOLUME INCREASED ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DEFORMITY ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DELIVERY ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DENTAL CARE ( 1 FDA reports)
DENTAL CARIES ( 1 FDA reports)
DENTAL OPERATION ( 1 FDA reports)
DETOXIFICATION ( 1 FDA reports)
DEVICE MALFUNCTION ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DROOLING ( 1 FDA reports)
DRUG DETOXIFICATION ( 1 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
ELECTRIC SHOCK ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
ELEVATED MOOD ( 1 FDA reports)
ENDOSCOPY SMALL INTESTINE ABNORMAL ( 1 FDA reports)
ENERGY INCREASED ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EXOPHTHALMOS ( 1 FDA reports)
EXPOSURE VIA SEMEN ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
FAECAL VOMITING ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FEELINGS OF WORTHLESSNESS ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
FOOD ALLERGY ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
GINGIVAL SWELLING ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GRUNTING ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMOCHROMATOSIS ( 1 FDA reports)
HAEMOGLOBINAEMIA ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATITIS VIRAL ( 1 FDA reports)
HEPATOBILIARY NEOPLASM ( 1 FDA reports)
HERPANGINA ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
HOSTILITY ( 1 FDA reports)
HYPERACUSIS ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPEREMESIS GRAVIDARUM ( 1 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOMANIA ( 1 FDA reports)
HYPOSMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
ILEUS ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
INAPPROPRIATE AFFECT ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFUSION SITE EXTRAVASATION ( 1 FDA reports)
INFUSION SITE INFECTION ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
INJECTION SITE WARMTH ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
INTESTINAL OPERATION ( 1 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 1 FDA reports)
JOINT FLUID DRAINAGE ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
JUGULAR VEIN THROMBOSIS ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LACTOSE INTOLERANCE ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIBIDO INCREASED ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIP ULCERATION ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LOGORRHOEA ( 1 FDA reports)
LOSS OF CONTROL OF LEGS ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LUPUS ENCEPHALITIS ( 1 FDA reports)
LUPUS ENTERITIS ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
LYMPHOEDEMA ( 1 FDA reports)
MASS ( 1 FDA reports)
MASTECTOMY ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
MENOPAUSE ( 1 FDA reports)
METANEPHRINE URINE INCREASED ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
METASTASES TO MENINGES ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
MIGRAINE WITH AURA ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MUCOUS STOOLS ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MULTIPLE ALLERGIES ( 1 FDA reports)
MULTIPLE INJURIES ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NASAL ULCER ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NECK INJURY ( 1 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 1 FDA reports)
NERVE COMPRESSION ( 1 FDA reports)
NERVE INJURY ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NORMETANEPHRINE URINE INCREASED ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
PALATAL DISORDER ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PANIC REACTION ( 1 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 1 FDA reports)
PARASOMNIA ( 1 FDA reports)
PARKINSONIAN GAIT ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PHALANGEAL AGENESIS ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PILOERECTION ( 1 FDA reports)
PLATELET ADHESIVENESS INCREASED ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POST PROCEDURAL INFECTION ( 1 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 1 FDA reports)
POSTPARTUM DEPRESSION ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
PRESBYOPIA ( 1 FDA reports)
PRESCRIPTION FORM TAMPERING ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROTEIN URINE ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
PUNCTURE SITE REACTION ( 1 FDA reports)
RADIAL NERVE PALSY ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
REBOUND EFFECT ( 1 FDA reports)
RECTAL TENESMUS ( 1 FDA reports)
RENAL COLIC ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
SCRATCH ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SELF-INJURIOUS IDEATION ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN FIBROSIS ( 1 FDA reports)
SKIN HYPERTROPHY ( 1 FDA reports)
SKIN INDURATION ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SKIN SWELLING ( 1 FDA reports)
SKIN TIGHTNESS ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SLUGGISHNESS ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
SMOKER ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SOCIAL PHOBIA ( 1 FDA reports)
SOMATOFORM DISORDER ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 1 FDA reports)
TENSION HEADACHE ( 1 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 1 FDA reports)
THOUGHT BLOCKING ( 1 FDA reports)
THROMBOPHLEBITIS MIGRANS ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 1 FDA reports)
TRISMUS ( 1 FDA reports)
TROPONIN I INCREASED ( 1 FDA reports)
TUMOUR MARKER INCREASED ( 1 FDA reports)
ULCER HAEMORRHAGE ( 1 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 1 FDA reports)
UTERINE MALPOSITION ( 1 FDA reports)
VAGINAL INFECTION ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VOLVULUS ( 1 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 1 FDA reports)
VULVOVAGINAL DRYNESS ( 1 FDA reports)
WEIGHT BEARING DIFFICULTY ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)

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