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

FATIGUE ( 53 FDA reports)
NAUSEA ( 44 FDA reports)
DRUG INEFFECTIVE ( 39 FDA reports)
DYSPNOEA ( 32 FDA reports)
HEADACHE ( 30 FDA reports)
PAIN ( 30 FDA reports)
DIARRHOEA ( 27 FDA reports)
ABDOMINAL PAIN ( 26 FDA reports)
BACK PAIN ( 25 FDA reports)
HYPERHIDROSIS ( 24 FDA reports)
WEIGHT INCREASED ( 24 FDA reports)
ANXIETY ( 23 FDA reports)
DEEP VEIN THROMBOSIS ( 22 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 22 FDA reports)
DIZZINESS ( 20 FDA reports)
CHEST DISCOMFORT ( 18 FDA reports)
PAIN IN EXTREMITY ( 18 FDA reports)
PRURITUS ( 18 FDA reports)
ASTHENIA ( 17 FDA reports)
COUGH ( 17 FDA reports)
ASTHMA ( 16 FDA reports)
BLOOD URINE PRESENT ( 16 FDA reports)
INSOMNIA ( 16 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 16 FDA reports)
PELVIC PAIN ( 16 FDA reports)
CYST ( 15 FDA reports)
PULMONARY EMBOLISM ( 15 FDA reports)
VOMITING ( 15 FDA reports)
FEELING ABNORMAL ( 14 FDA reports)
HYPERSENSITIVITY ( 14 FDA reports)
NECK PAIN ( 14 FDA reports)
SINUSITIS ( 14 FDA reports)
HYPERTENSION ( 13 FDA reports)
INJECTION SITE PAIN ( 13 FDA reports)
RASH ( 13 FDA reports)
ABDOMINAL PAIN UPPER ( 12 FDA reports)
CHEST PAIN ( 12 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 12 FDA reports)
SOMNOLENCE ( 12 FDA reports)
ARRESTED LABOUR ( 11 FDA reports)
PARAESTHESIA ( 11 FDA reports)
AMNESIA ( 10 FDA reports)
BLOOD PRESSURE INCREASED ( 10 FDA reports)
HEART RATE INCREASED ( 10 FDA reports)
TREMOR ( 10 FDA reports)
WEIGHT DECREASED ( 10 FDA reports)
BLOOD GLUCOSE INCREASED ( 9 FDA reports)
DECREASED APPETITE ( 9 FDA reports)
FEAR ( 9 FDA reports)
INJURY ( 9 FDA reports)
RENAL CYST ( 9 FDA reports)
VISION BLURRED ( 9 FDA reports)
WHEEZING ( 9 FDA reports)
ANHEDONIA ( 8 FDA reports)
ARTHRALGIA ( 8 FDA reports)
BRONCHITIS ( 8 FDA reports)
CORONARY ARTERY OCCLUSION ( 8 FDA reports)
EMOTIONAL DISTRESS ( 8 FDA reports)
FALL ( 8 FDA reports)
FLUSHING ( 8 FDA reports)
NERVOUSNESS ( 8 FDA reports)
OEDEMA PERIPHERAL ( 8 FDA reports)
PALPITATIONS ( 8 FDA reports)
STILLBIRTH ( 8 FDA reports)
URINARY TRACT INFECTION ( 8 FDA reports)
URTICARIA ( 8 FDA reports)
ABDOMINAL DISCOMFORT ( 7 FDA reports)
ANAEMIA ( 7 FDA reports)
CHOLECYSTITIS CHRONIC ( 7 FDA reports)
ERYTHEMA ( 7 FDA reports)
EYE PAIN ( 7 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 7 FDA reports)
HYPERSOMNIA ( 7 FDA reports)
LACUNAR INFARCTION ( 7 FDA reports)
MALAISE ( 7 FDA reports)
MIGRAINE ( 7 FDA reports)
MUSCLE SPASMS ( 7 FDA reports)
MYOCARDIAL INFARCTION ( 7 FDA reports)
OROPHARYNGEAL PAIN ( 7 FDA reports)
PRODUCT QUALITY ISSUE ( 7 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 7 FDA reports)
PYREXIA ( 7 FDA reports)
RESPIRATORY TRACT CONGESTION ( 7 FDA reports)
BLOOD POTASSIUM DECREASED ( 6 FDA reports)
CATARACT ( 6 FDA reports)
CONFUSIONAL STATE ( 6 FDA reports)
DEPRESSION ( 6 FDA reports)
DYSPEPSIA ( 6 FDA reports)
DYSPNOEA EXERTIONAL ( 6 FDA reports)
FLUID RETENTION ( 6 FDA reports)
INJECTION SITE ERYTHEMA ( 6 FDA reports)
MUSCULAR WEAKNESS ( 6 FDA reports)
MYALGIA ( 6 FDA reports)
THROMBOSIS ( 6 FDA reports)
ANAPHYLACTIC REACTION ( 5 FDA reports)
ANOSMIA ( 5 FDA reports)
BLISTER ( 5 FDA reports)
CANDIDIASIS ( 5 FDA reports)
CHILLS ( 5 FDA reports)
EYE SWELLING ( 5 FDA reports)
FEELING HOT ( 5 FDA reports)
GALLBLADDER INJURY ( 5 FDA reports)
HOT FLUSH ( 5 FDA reports)
HYPOAESTHESIA ( 5 FDA reports)
HYPOKALAEMIA ( 5 FDA reports)
MEMORY IMPAIRMENT ( 5 FDA reports)
MUSCULOSKELETAL PAIN ( 5 FDA reports)
NASOPHARYNGITIS ( 5 FDA reports)
PANCREATITIS ( 5 FDA reports)
PHOTOSENSITIVITY REACTION ( 5 FDA reports)
RHINORRHOEA ( 5 FDA reports)
SCAR ( 5 FDA reports)
SPINAL DISORDER ( 5 FDA reports)
SUICIDE ATTEMPT ( 5 FDA reports)
ABDOMINAL DISTENSION ( 4 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
CEREBROVASCULAR ACCIDENT ( 4 FDA reports)
CHROMATURIA ( 4 FDA reports)
COAGULOPATHY ( 4 FDA reports)
COLITIS ISCHAEMIC ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
CRYING ( 4 FDA reports)
DEHYDRATION ( 4 FDA reports)
DISTURBANCE IN ATTENTION ( 4 FDA reports)
DRUG EFFECT DECREASED ( 4 FDA reports)
DRUG INTERACTION ( 4 FDA reports)
DRY MOUTH ( 4 FDA reports)
DYSKINESIA ( 4 FDA reports)
DYSMENORRHOEA ( 4 FDA reports)
DYSPHONIA ( 4 FDA reports)
EAR INFECTION ( 4 FDA reports)
FACTOR VIII DEFICIENCY ( 4 FDA reports)
FEELING COLD ( 4 FDA reports)
FOOT FRACTURE ( 4 FDA reports)
HEPATOMEGALY ( 4 FDA reports)
HYPERACUSIS ( 4 FDA reports)
HYPOTENSION ( 4 FDA reports)
INCORRECT DOSE ADMINISTERED ( 4 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 4 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 4 FDA reports)
MEDICATION ERROR ( 4 FDA reports)
MENTAL DISORDER ( 4 FDA reports)
NASAL CONGESTION ( 4 FDA reports)
OCULAR ICTERUS ( 4 FDA reports)
PEPTIC ULCER ( 4 FDA reports)
PERSONALITY CHANGE ( 4 FDA reports)
PLEURAL EFFUSION ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
PSORIASIS ( 4 FDA reports)
PSYCHIATRIC SYMPTOM ( 4 FDA reports)
PULSE ABNORMAL ( 4 FDA reports)
RECTAL HAEMORRHAGE ( 4 FDA reports)
RENAL PAIN ( 4 FDA reports)
SUICIDAL IDEATION ( 4 FDA reports)
TACHYCARDIA ( 4 FDA reports)
TENDERNESS ( 4 FDA reports)
THROAT TIGHTNESS ( 4 FDA reports)
URINARY INCONTINENCE ( 4 FDA reports)
ABDOMINAL PAIN LOWER ( 3 FDA reports)
ACCIDENTAL EXPOSURE ( 3 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 3 FDA reports)
ACUTE HEPATIC FAILURE ( 3 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 3 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 3 FDA reports)
ASCITES ( 3 FDA reports)
BEDRIDDEN ( 3 FDA reports)
BREAST PAIN ( 3 FDA reports)
BURNING SENSATION ( 3 FDA reports)
CELLULITIS ( 3 FDA reports)
CHOKING ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
CONTUSION ( 3 FDA reports)
COSTOCHONDRITIS ( 3 FDA reports)
DERMATITIS ACNEIFORM ( 3 FDA reports)
DRUG DISPENSING ERROR ( 3 FDA reports)
DRY EYE ( 3 FDA reports)
DRY SKIN ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
DYSURIA ( 3 FDA reports)
EMOTIONAL DISORDER ( 3 FDA reports)
ENCEPHALOPATHY ( 3 FDA reports)
EPISTAXIS ( 3 FDA reports)
EXPIRED DRUG ADMINISTERED ( 3 FDA reports)
EYE PRURITUS ( 3 FDA reports)
FAT REDISTRIBUTION ( 3 FDA reports)
GOITRE ( 3 FDA reports)
HAEMORRHOIDS ( 3 FDA reports)
HEPATIC CIRRHOSIS ( 3 FDA reports)
HEPATIC STEATOSIS ( 3 FDA reports)
HYPOCALCAEMIA ( 3 FDA reports)
IMPAIRED WORK ABILITY ( 3 FDA reports)
INFLUENZA ( 3 FDA reports)
INJECTION SITE HAEMATOMA ( 3 FDA reports)
INJECTION SITE SWELLING ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
JOINT STIFFNESS ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
LIVER TRANSPLANT REJECTION ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
MENORRHAGIA ( 3 FDA reports)
NASAL DISCOMFORT ( 3 FDA reports)
NEPHROPATHY TOXIC ( 3 FDA reports)
NEUROPATHY ( 3 FDA reports)
NEUROTOXICITY ( 3 FDA reports)
NEUTROPENIA ( 3 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 3 FDA reports)
OFF LABEL USE ( 3 FDA reports)
OSTEOPOROSIS ( 3 FDA reports)
PANIC ATTACK ( 3 FDA reports)
POLYHYDRAMNIOS ( 3 FDA reports)
POST PROCEDURAL HAEMATOMA ( 3 FDA reports)
PROTHROMBIN TIME PROLONGED ( 3 FDA reports)
RESPIRATORY TRACT INFECTION ( 3 FDA reports)
SKIN DISORDER ( 3 FDA reports)
SKIN LACERATION ( 3 FDA reports)
SLEEP APNOEA SYNDROME ( 3 FDA reports)
SLEEP DISORDER ( 3 FDA reports)
SNEEZING ( 3 FDA reports)
STOMACH DISCOMFORT ( 3 FDA reports)
SWELLING ( 3 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 3 FDA reports)
THROMBOCYTHAEMIA ( 3 FDA reports)
VEIN DISORDER ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ABNORMAL DREAMS ( 2 FDA reports)
ACNE ( 2 FDA reports)
ADNEXA UTERI PAIN ( 2 FDA reports)
ADVERSE EVENT ( 2 FDA reports)
AGEUSIA ( 2 FDA reports)
AMENORRHOEA ( 2 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 2 FDA reports)
ANTISOCIAL BEHAVIOUR ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 2 FDA reports)
AUTOIMMUNE DISORDER ( 2 FDA reports)
BLINDNESS ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD PH INCREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
BREAST DISORDER ( 2 FDA reports)
BREAST MASS ( 2 FDA reports)
BREAST TENDERNESS ( 2 FDA reports)
BRONCHOSPASM ( 2 FDA reports)
CAESAREAN SECTION ( 2 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 2 FDA reports)
CERVICOBRACHIAL SYNDROME ( 2 FDA reports)
CERVIX DISORDER ( 2 FDA reports)
CHOLECYSTECTOMY ( 2 FDA reports)
CHOLESTEROSIS ( 2 FDA reports)
CLUSTER HEADACHE ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
DEATH ( 2 FDA reports)
DEPRESSION SUICIDAL ( 2 FDA reports)
DERMATITIS CONTACT ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
DRUG DOSE OMISSION ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
ECONOMIC PROBLEM ( 2 FDA reports)
EPIGASTRIC DISCOMFORT ( 2 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 2 FDA reports)
FAECES PALE ( 2 FDA reports)
FAILED INDUCTION OF LABOUR ( 2 FDA reports)
FAMILY STRESS ( 2 FDA reports)
FEELING JITTERY ( 2 FDA reports)
FOETAL ALCOHOL SYNDROME ( 2 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 2 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 2 FDA reports)
GALLBLADDER DISORDER ( 2 FDA reports)
GASTRIC DISORDER ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GINGIVAL BLEEDING ( 2 FDA reports)
GINGIVAL SWELLING ( 2 FDA reports)
GRIP STRENGTH DECREASED ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 2 FDA reports)
HOUSE DUST ALLERGY ( 2 FDA reports)
HYPERTHYROIDISM ( 2 FDA reports)
HYPOCOAGULABLE STATE ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 2 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 2 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
INJECTION SITE IRRITATION ( 2 FDA reports)
IRRITABLE BOWEL SYNDROME ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
KIDNEY INFECTION ( 2 FDA reports)
LACRIMATION INCREASED ( 2 FDA reports)
LEARNING DISABILITY ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LIPASE INCREASED ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
MASTOIDITIS ( 2 FDA reports)
MENISCUS LESION ( 2 FDA reports)
MOOD SWINGS ( 2 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 2 FDA reports)
MYOPATHY STEROID ( 2 FDA reports)
ODYNOPHAGIA ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OESOPHAGEAL PAIN ( 2 FDA reports)
OSTEONECROSIS ( 2 FDA reports)
PAINFUL RESPIRATION ( 2 FDA reports)
PALLOR ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
PREGNANCY ( 2 FDA reports)
PROTEIN TOTAL DECREASED ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
RHEUMATOID LUNG ( 2 FDA reports)
RHINITIS ( 2 FDA reports)
SENSORY DISTURBANCE ( 2 FDA reports)
SERUM SICKNESS ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
SKIN BURNING SENSATION ( 2 FDA reports)
SKIN EXFOLIATION ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
SUFFOCATION FEELING ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
TARDIVE DYSKINESIA ( 2 FDA reports)
TEMPERATURE REGULATION DISORDER ( 2 FDA reports)
THROAT IRRITATION ( 2 FDA reports)
THYROID DISORDER ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
TONGUE DISORDER ( 2 FDA reports)
UNDERDOSE ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
VAGINAL INFECTION ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
VICTIM OF SEXUAL ABUSE ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
ABNORMAL FAECES ( 1 FDA reports)
ACCIDENTAL NEEDLE STICK ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
ALLERGIC COLITIS ( 1 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ANGER ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 1 FDA reports)
ANTITHROMBIN III INCREASED ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APPENDICITIS PERFORATED ( 1 FDA reports)
APPLICATION SITE DISCHARGE ( 1 FDA reports)
APPLICATION SITE IRRITATION ( 1 FDA reports)
APPLICATION SITE RASH ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
APPLICATION SITE URTICARIA ( 1 FDA reports)
APPLICATION SITE VESICLES ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ARTHROPOD BITE ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 1 FDA reports)
B-CELL LYMPHOMA ( 1 FDA reports)
BARRETT'S OESOPHAGUS ( 1 FDA reports)
BILIARY DYSKINESIA ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BIPOLAR I DISORDER ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD GASES ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD PRESSURE ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLUNTED AFFECT ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BONE DENSITY DECREASED ( 1 FDA reports)
BRACHYTHERAPY ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BRAIN STEM STROKE ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CAROTID ARTERY DISEASE ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CERVICAL SPINAL STENOSIS ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHOREA ( 1 FDA reports)
CHORIORETINAL DISORDER ( 1 FDA reports)
CHORIORETINOPATHY ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
CONGENITAL MUSCULOSKELETAL ANOMALY ( 1 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 1 FDA reports)
DEFORMITY ( 1 FDA reports)
DEMYELINATION ( 1 FDA reports)
DEVICE MALFUNCTION ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DISINHIBITION ( 1 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPHEMIA ( 1 FDA reports)
DYSPLASIA ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
EAR DISCOMFORT ( 1 FDA reports)
EAR DISORDER ( 1 FDA reports)
EAR PRURITUS ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
ELECTRON RADIATION THERAPY TO PROSTATE ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
FACIAL PAIN ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FEAR OF DEATH ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 1 FDA reports)
FEELING OF DESPAIR ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FOREIGN BODY ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GALLBLADDER OPERATION ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
GLAUCOMATOUS OPTIC DISC ATROPHY ( 1 FDA reports)
GLIOSIS ( 1 FDA reports)
GLOSSITIS ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HAEMANGIOMA OF LIVER ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEPATIC CYST ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HODGKIN'S DISEASE ( 1 FDA reports)
HORMONE LEVEL ABNORMAL ( 1 FDA reports)
HYPERMOBILITY SYNDROME ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOMANIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOTRICHOSIS ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
INCISION SITE CELLULITIS ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INCORRECT PRODUCT STORAGE ( 1 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 1 FDA reports)
INFUSION SITE PAIN ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE NODULE ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
INTESTINAL SPASM ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
IRITIS ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
JAW DISORDER ( 1 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LABOUR ONSET DELAYED ( 1 FDA reports)
LARYNGITIS ( 1 FDA reports)
LAZINESS ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LIBIDO DECREASED ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LOGORRHOEA ( 1 FDA reports)
LUMBAR PUNCTURE HEADACHE ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
LYMPHOCYTOSIS ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MACULAR DEGENERATION ( 1 FDA reports)
MAJOR DEPRESSION ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MENTALLY LATE DEVELOPER ( 1 FDA reports)
METAPLASIA ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NASAL SINUS DRAINAGE ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NEURODEVELOPMENTAL DISORDER ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE III ( 1 FDA reports)
NONSPECIFIC REACTION ( 1 FDA reports)
NYSTAGMUS ( 1 FDA reports)
OCULAR HYPERTENSION ( 1 FDA reports)
ONYCHALGIA ( 1 FDA reports)
ONYCHOCLASIS ( 1 FDA reports)
OPEN ANGLE GLAUCOMA ( 1 FDA reports)
OPHTHALMOPLEGIA ( 1 FDA reports)
OPTIC ATROPHY ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
ORAL PRURITUS ( 1 FDA reports)
OROPHARYNGEAL BLISTERING ( 1 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PAINFUL DEFAECATION ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COUNTERFEIT ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PLEURAL FIBROSIS ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PNEUMONIA BACTERIAL ( 1 FDA reports)
PO2 INCREASED ( 1 FDA reports)
POST CONCUSSION SYNDROME ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POSTURAL ORTHOSTATIC TACHYCARDIA SYNDROME ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROSTATIC DISORDER ( 1 FDA reports)
PROTEIN C DEFICIENCY ( 1 FDA reports)
PROTEIN S INCREASED ( 1 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 1 FDA reports)
PULMONARY INFARCTION ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RAYNAUD'S PHENOMENON ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RENAL ARTERY OCCLUSION ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RETINAL DEGENERATION ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SCOLIOSIS ( 1 FDA reports)
SCOTOMA ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SEASONAL ALLERGY ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
SEXUAL DYSFUNCTION ( 1 FDA reports)
SICCA SYNDROME ( 1 FDA reports)
SIMPLE PARTIAL SEIZURES ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SKELETAL INJURY ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SPINAL COLUMN STENOSIS ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 1 FDA reports)
TACHYPHRENIA ( 1 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 1 FDA reports)
TENDON PAIN ( 1 FDA reports)
TENDONITIS ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THIRST ( 1 FDA reports)
THROAT LESION ( 1 FDA reports)
THROMBIN-ANTITHROMBIN III COMPLEX ABNORMAL ( 1 FDA reports)
TIBIA FRACTURE ( 1 FDA reports)
TONGUE DESQUAMATION ( 1 FDA reports)
TONGUE DISCOLOURATION ( 1 FDA reports)
TONGUE ULCERATION ( 1 FDA reports)
TOOTH FRACTURE ( 1 FDA reports)
TRAUMATIC BRAIN INJURY ( 1 FDA reports)
TRICHORRHEXIS ( 1 FDA reports)
TRIGGER FINGER ( 1 FDA reports)
TRISMUS ( 1 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 1 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 1 FDA reports)
URETHRAL STENOSIS ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
URINE COLOUR ABNORMAL ( 1 FDA reports)
UTERINE CERVICAL PAIN ( 1 FDA reports)
VAGINAL BURNING SENSATION ( 1 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
VITREOUS FLOATERS ( 1 FDA reports)
VULVAL OEDEMA ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)

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